Category: 2576-47-8

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Organic compounds having carbon bonded to bromine are called organic bromides. HPLC of Formula: 2576-47-8.

Lu, Pingping;He, Shuai;Zhou, Yue;Zhang, Yongmin research published 《 Oxidation-Induced Breakage of the Imine Bond and Aggregate Transition in a Se-Containing Dynamic Covalent Surfactant》, the research content is summarized as follows. Controlling the dynamic imine bonds upon a novel trigger except for pH and temperature is still a significant challenge. Here, a Se-containing imine-based dynamic covalent surfactant (HOBAB-BSeEA) was developed for the first time by mixing two precursors in situ: an asym. double-chain cationic surfactant bearing a formyl group at the terminal of one hydrophobic tail and a Se-containing amine (2-(benzylselanyl)ethan-1-amine) in order to confirm the effect of redox on the imine bonds. The imine bond in HOBAB-BSeEA can be regulated not only upon changing the pH as well as other common imine-based surfactants but also by oxidation The conversion efficiency of imine bonds is closely related with the degree of oxidation and pH. Complete oxidation can decrease the conversion efficiency from ~87 to 48%, which is comparable to the result of changing the pH from 10.0 to 7.0. With the formation and breaking of imine bonds, the surfactant can be reversibly switched between sym. and asym. structures, accompanied by a morphol. transition from vesicles to spherical micelles. Although oxidation cannot demolish all imine bonds, it can completely convert vesicles to spherical micelles, which is mainly ascribed to an increase in the polarity of the micellar microenvironment stemming from the oxidation of Se. However, this transition can only be achieved by reducing the pH to 5.0 instead of 7.0. Nile red loaded in HOBAB-BSeEA vesicles can be quickly, controllably, and step-by-step released upon oxidation stimulus but not pH. Understanding the mechanism of oxidation-induced breakage of imine bonds and disruption of vesicles would be useful in designing redox-responsive imine-based carriers that can unload cargoes according to the level of the local reactive oxygen species.

HPLC of Formula: 2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., 2576-47-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. HPLC of Formula: 2576-47-8.

Ma, Lie;Zhang, Chi;Lin, Saisai;Chen, Shengfu;Yao, Zhikan;Sun, Zhilin;Gao, Congjie;Zhang, Lin research published 《 Enhancing antifouling property of reverse osmosis membranes via surface tethered with the aminated cation of ionic liquids》, the research content is summarized as follows. The elec. neutrality of ionic liquids (ILs) was exploited to enhance the antifouling property of polyamide (PA) reverse osmosis (RO) membranes in this work. We solely tethered the aminated imidazolium cation of ILs [AVIM] Br onto the top-surface of PA RO membranes via mild amidation. The mol. simulation results confirmed that the tethered imidazolium cation and the dissociated bromine anion were stably existed in the form of ion pairs on PA RO membrane surface. In virtue of the elec. neutrality of these ion pairs, the ionic-solvation induced hydration layer formed in ILs above the modified membrane surface was thick and evenly distributed, similar to that formed in conventionally electroneutral zwitterion antifouling materials. Thereby, the cation-tethered membrane surface intuitively achieved balanced charge and strong hydrophilicity, and stably exhibited low protein adsorption and excellent antifouling behaviors to diverse foulants, even when the imidazolium cation was paired with anions of different mol. size. Meanwhile, the typical ridge-and-valley surface morphol. for PA RO membrane was well preserved due to the mild modification condition, and thereby harvested satisfactory separation performance. The integration of high performance, abundant ILs and mild conditions was expected to expand the application of superb antifouling materials in a variety of biofouling areas.

2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., HPLC of Formula: 2576-47-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Organobromine compounds have fallen under increased scrutiny for their environmental impact., HPLC of Formula: 2576-47-8.

Maegawa, Koshiro;Tanimoto, Hiroki;Onishi, Seiji;Tomohiro, Takenori;Morimoto, Tsumoru;Kakiuchi, Kiyomi research published 《 Taming the reactivity of alkyl azides by intramolecular hydrogen bonding: site-selective conjugation of unhindered diazides》, the research content is summarized as follows. Organic azides are still in the center of click chem. connecting two mols. However, taming the conjugation selectivity of azides is difficult without the help of bulky groups. Herein the unique reactivities of α-azido secondary acetamides (α-AzSAs) as minimal and unhindered azide structures is reported. The NH-azide interaction in the α-AzSAs, supposed by DFT calculations, allowed selective conjugation in the presence of other azido moieties, even without steric hindrance. With Staudinger-Bertozzi ligation, α-AzSAs underwent conjugation prior to the other primary alkyl azides. On the other hand, in propargyl cation-mediated triazole synthesis, other alkyl azides, including tertiary alkyl azides, underwent the conjugation faster than α-AzSAs. Authors also demonstrated site-selective integration of the functional components onto the diazide modular hubs.

HPLC of Formula: 2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., 2576-47-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide, Electric Literature of 2576-47-8

Linciano, Pasquale;Sorbi, Claudia;Comitato, Antonella;Lesniak, Anna;Bujalska-Zadrozny, Magdalena;Pawlowska, Agata;Bielenica, Anna;Orzelska-Gorka, Jolanta;Kedzierska, Ewa;Biala, Grazyna;Ronsisvalle, Simone;Limoncella, Silvia;Casarini, Livio;Cichero, Elena;Fossa, Paola;Satala, Grzegorz;Bojarski, Andrzej J.;Brasili, Livio;Bardoni, Rita;Franchini, Silvia research published 《 Identification of a Potent and Selective 5-HT_1A Receptor Agonist with In Vitro and In Vivo Antinociceptive Activity》, the research content is summarized as follows. Opioids are the gold standard drugs for the treatment of acute and chronic severe pain, although their serious side effects constitute a big limitation. In the search for new and safer drugs, 5-HT_1AR agonists are emerging as potential candidates in pain relief therapy. In this work, we evaluated the affinity and activity of enantiomers of the two newly synthesized, potent 5-HT_1AR agonists N-[(2,2-diphenyl-1,3-dioxolan-4-yl)methyl]-2-[2-(pyridin-4-yl)phenoxy]ethan-1-ammonium hydrogenoxalate (rac-1) and N-((2,2-diphenyl-1,3-dioxolan-4-yl)methyl)-2-(2-(1-methyl-1H-imidazol-5-yl)phenoxy)ethan-1-ammonium hydrogenoxalate (rac-2) in vitro and in vivo. The role of chirality in the interaction with 5-HT_1AR was evaluated by mol. docking. The activity of the rac-1 was tested in mouse models of acute pain (hot plate) and severe tonic nociceptive stimulation (intraplantar formalin test). Rac-1 was active in the formalin test with a reduction in paw licking in both phases at 10 mg/kg, and its effect was abolished by the selective 5-HT_1AR antagonist, WAY-100635. The eutomer (S)-1, but not the racemate, was active during the hot plate test at 10 and 20 mg/kg, and this effect was abolished by 30 min treatment with WAY-100635 at 30 min. Similarly to 8-OH-DPAT, (S)-1 evoked a slow outward current and depressed spontaneous glutamatergic transmission in superficial dorsal horn neurons, more effectively than rac-1. The eutomer (S)-1 showed promising developability properties, such as high selectivity over 5-HT subtypes, no interaction with the μ receptors, and low hepato- and cardiotoxicity. Therefore, (S)-1 may represent a potential candidate for the treatment of acute and chronic pain without having the adverse effects that are commonly associated with the classic opioid drugs.

Electric Literature of 2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., 2576-47-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Quality Control of 2576-47-8.

Liu, Chao;Yin, Qing;Zhang, Wenbo;Bao, Yan;Li, Peipei;Hao, Lifen;Ma, Jianzhong research published 《 Tribological properties of graphene-modified with ionic liquids and carbon quantum dots/ bismaleimide composites》, the research content is summarized as follows. In order to improve the tribol. properties of graphene reinforced polymer composites, ionic liquids (IL) and carbon quantum dots (CQDs) were deposited on the reduced graphene oxide (rGO) nanosheets surface to ameliorate the compatibility between graphene and bismaleimide (BMI) matrix, as well as the stability of their self-lubricating transfer films. Their tribol. properties were evaluated, and the wear mechanism was studied by means of surface/interface anal., resp. It could be found that CQDs/IL/rGO could improve the stability of the friction coefficient and decrease the volume wear rate of their BMI composites. When the filler amount was only 0.6 wt%, the friction coefficient and volume wear rate of CQDs/IL/rGO/BMI composites decreased by 41.2% and 94.7% compared with the neat BMI, resp. Also, the CQDs/IL/rGO/BMI composites exhibited the lowest friction coefficient fluctuations and volume wear rate than those of other composites. Because of the synergistic effects of the CQDs, IL and rGO, uniform, continuous and steady self-lubricating transfer film could be formed during the friction process, thus significantly improving the anti-friction and wear-resistance properties of CQDs/IL/rGO/BMI composites. More importantly, the unique combinations of advantages of each functional component can also be applied in many other fields, such as catalysis, chem. sensors, etc.

Quality Control of 2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., 2576-47-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Recommanded Product: 2-Bromoethylamine hydrobromide.

Li, Jie;Liu, Shu-lei;Yi, Qun;Li, Xiang-yuan;Li, Jian-chuan;Shi, Li-juan;Li, Jun research published 《 Effect of poly(ionic liquid)-based metal complexes on catalytic performance of cycloaddition reaction of CO₂ with epichlorohydrin》, the research content is summarized as follows. Based on the metal-coordination interaction between amino functionalized poly(ionic liquid)-NH₂ and Zn²⁺, a poly(ionic liquid)-based metal complex PIL-Zn with Lewis acid-base sites was assembled at room temperature, and its catalytic performance for the reaction of CO₂ and epichlorohydrin to synthesize chloropropylene carbonate was studied. Through the synergistic effect of acid-base sites (Br^–, Zn²⁺), PIL-Zn can effectively catalyze the conversion of CO₂ under the mild conditions (0.1 MPa, 75°C, 24 h) in the absence of solvent and co-catalyst, the conversion of epichlorohydrin and the selectivity of the target product chloropropylene carbonate are 95% and 99% resp., and its catalytic performance keeps well after 5 recycles. PIL-Zn exhibits good application potential in the field of catalytic conversion of CO₂, which provides a new idea for the development of high performance catalyst materials.

2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., Recommanded Product: 2-Bromoethylamine hydrobromide

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide, Electric Literature of 2576-47-8

Li, Jun;Hu, Zu-E.;Yang, Xian-Ling;Zhang, Meng-Qian;Liu, Yan-Hong;Wang, Na;Yu, Xiao-Qi research published 《 Hierarchical Targeted Delivery of Lonidamine and Camptothecin Based on the Ultra-Rapid pH/GSH Response Nanoparticles for Synergistic Chemotherapy》, the research content is summarized as follows. A facile strategy to construct dual-drug delivery nanoparticles (TL-CPT NPs), which possessed higher loading content of CPT and TPP-LND. Notably, TL-CPT NPs showed promising ultrarapid pH/GSH response to release more than 86% of loaded TPP-LND or 93% of loaded CPT in just 2 h. The results showed that the nanoparticles hierarchically delivered CPT and TPP-LND to targeted different organelles without mutual influence benefiting the ultrarapid pH/GSH response to drug release, and further significantly and synergistically induced cell apoptosis and improved chemotherapeutic efficiency in cancer cells.

2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., Electric Literature of 2576-47-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

One prominent application of synthetic organobromine compounds is the use of polybrominated diphenyl ethers as fire-retardants, and in fact fire-retardant manufacture is currently the major industrial use of the element bromine. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide, Quality Control of 2576-47-8

Li, Gefei;Zhang, Yong;Wang, Wenhui;Gao, Lei;Ren, Yukun;Che, Junyan;Mo, Chunjing;Liu, Hongwei;Zhao, Weijie;Lu, Junpeng;Ni, Zhenhua research published 《 Correlated Dynamics of Free and Self-Trapped Excitons and Broadband Photodetection in BEA₂PbBr₄ Layered Crystals》, the research content is summarized as follows. Self-trapped excitons (STEs) exert a profound impact on the optical properties and device applications of 2D halide perovskites. Particularly distinct exciton self-trapping and detrapping processes can facilitate the intelligent design of perovskite optoelectronic devices with emerging functionalities. Thus, a comprehensive understanding and regulation of exciton trapping and detrapping dynamics are highly desired. Herein, the authors report a 2D lead halide perovskite (BEA₂PbBr₄ where BEA is 2-bromine ethylamine) with exceptional broadband photoluminescence (PL), which originates from multiple STE states. In particular, the unique energy-level configuration of STEs with respect to free excitons is revealed by exploiting optical spectroscopy. Consequently, these distinct phenomena empower the broadband photodetection capability of BEA₂PbBr₄ photodetectors over a wide range from UV to near-IR wavelengths. These results provide an essential understanding of the intriguing photophysics of STEs and shed new light on the future development of single-component perovskite broadband optoelectronic devices.

Quality Control of 2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., 2576-47-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Product Details of C2H7Br2N.

Kertsomboon, Thanit;Chirachanchai, Suwabun research published 《 Amphiphilic biodegradable co-networks of Poly(butylene succinate)-Poly(ethylene glycol) chains for nano-gelation via Click chemistry and its potential dispersant for multi-walled carbon nanotubes》, the research content is summarized as follows. Amphiphilic nanogel (APNG) is a class of material miscible with water and oil which is practical for active mols. incorporation, water-oil dispersion, etc. In general, preparation of APNGs requires multi-steps involving the copolymer with different hydrophilic units and the micelles formation to confine the nano-level for the crosslink. The present work proposes a simple way to prepare APNGs by applying the co-networks of biodegradable hydrophilic and hydrophobic chains. The co-networks between alkyno-poly(acrylic acid) (alkyno-PAA) and diazido-poly(ethylene glycol) (N₃-PEG-N₃) as well as diazido-poly(butylene succinate) (N₃-PBS-N₃) via copper-catalyzed azide-alkyne cycloaddition (CuAAC) Click lead to APNG. The variation of hydrophilic N₃-PEG-N₃ and hydrophobic N₃-PBS-N₃ controls the amphiphilicity as evidenced from the swelling performances in various solvents with different polarity. The APNG obtained favors multi-walled carbon nanotubes (MWCNTs) to be dispersed in water for weeks without precipitation suggesting a potential dispersant of MWCNTs in hydrophilic media, especially aqueous solution

Product Details of C2H7Br2N, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., 2576-47-8.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. SDS of cas: 2576-47-8.

Kadafour, Attahir N. W.;Bala, Muhammad D. research published 《 Structural characterization of a square planar Ni(II) complex and its application as a catalyst for the transfer hydrogenation of ketones》, the research content is summarized as follows. A new 2-hydroxy-1-naphthaldehyde Schiff base derived nickel(II) complex (4) was synthesized and fully characterized. Anal. of the structure of 4 by single-crystal X-ray diffraction shows two chelating Schiff base ligands bound to nickel in a trans [O^ΛN(Ni²⁺)N^ΛO] fashion. Hence, in a mol. of 4, two ligands are four coordinate to a Ni(II) center through the imine nitrogen and naphthyloxyl oxygen atoms. This coordination mode resulted in a square planar complex that is stabilized in the solid-state by a network of intermol. O-H···N hydrogen bonds between neighboring mols. The ¹H NMR data showed the loss of the hydroxyl (OH) proton signal and an upfield shift of the metal-bound imine (-NH) proton signal, while the IR data also showed a lower energy shift in the absorption frequency of the imine (C = N) bond due to back donation from the coordinated Ni(II) center. As a catalyst for the transfer hydrogenation of a range of ketones, 4 showed good catalytic activity at a very low concentration of 0.1 mol% with 2-propanol as the model substrate. The catalyst is also effective for various related ketone substrates bearing a range of steric and electronic regulating groups.

2576-47-8, 2-Bromoethylamine hydrobromide is a useful building block for proteomics research.
2-Bromoethylamine hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist. It is used to construct C2-symmetric imidazolidinylidene ligands with a dioxolane backbone.
2-Bromoethylamine Hydrobromide is used in the synthesis of analogs of 5,​10,​15,​20-​tetrakis(1-​methylpyridinium-​4-​yl)​porphyrin (TMPyP4) as inhibitors of human telomerase. It is also used to prepare SB-705498, a potent, selective and orally bioavailable TRPV1 antagonist.
2-Bromoethylamine hydrobromide is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It is a prodrug that is hydrolyzed in vivo to its active form, 2-Bromoethylamine hydrobromide. The bound form of this drug has been shown to inhibit the development of cell nuclei in the nucleus of cells. This drug also inhibits the production of nitric oxide, which leads to cell death by necrosis. 2-Bromoethylamine hydrobromide has been shown to have an inhibitory effect on the activity of glycol ethers, which are used as solvents for resins in coatings and adhesives., SDS of cas: 2576-47-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary