Category: 1575-37-7

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Recommanded Product: 4-Bromobenzene-1,2-diamine.

Gillespie, James E.;Morrill, Charlotte;Phipps, Robert J. research published �Regioselective Radical Arene Amination for the Concise Synthesis of ortho-Phenylenediamines� the research content is summarized as follows. The formation of arene C-N bonds directly from C-H bonds is of great importance and there has been rapid recent development of methods for achieving this through radical mechanisms, often involving reactive N-centered radicals. A major challenge associated with these advances is that of regiocontrol, with mixtures of regioisomeric products obtained in most protocols, limiting broader utility. We have designed a system that utilizes attractive noncovalent interactions between an anionic substrate and an incoming radical cation in order to guide the latter to the arene ortho position. The anionic substrate takes the form of a sulfamate-protected aniline and telescoped cleavage of the sulfamate group after amination leads directly to ortho-phenylenediamines, key building blocks for a range of medicinally relevant diazoles. Our method can deliver both free amines and monoalkyl amines allowing access to unsym., selectively monoalkylated benzimidazoles and benzotriazoles. As well as providing concise access to valuable ortho-phenylenediamines, this work demonstrates the potential for utilizing noncovalent interactions to control positional selectivity in radical reactions.

Recommanded Product: 4-Bromobenzene-1,2-diamine, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., 1575-37-7.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Related Products of 1575-37-7.

Gong, Kai;Li, Cunhao;Zhang, Daquan;Lu, Huilin;Wang, Yunyun;Li, Haoran;Zhang, Huimin research published ã€?Sulfonic acid functionalized covalent organic frameworks as efficient catalyst for the one-pot tandem reactionsã€? the research content is summarized as follows. A covalent organic framework containing hydroxyl groups (HO-COF) has been predesigned and synthesized by the cyclotrimerization reaction of acetyls, which was used as a pre-established network to introduce Pr sulfonic acid through post-synthetic modification strategy, for the fabrication of SO₃H-COF with graphene-like multilayer structure. SO₃H-COF was employed as an effective heterogeneous catalyst for the synthesis of benzimidazoles, the synthesis of benzodiazepines and one-pot reductive amination of carbonyl compounds The results indicated that the developed protocol has several advantages, such as high activity, broad substrate scope, short reaction time and excellent yields. The distinctive structures of SO₃H-COF endowed the fantastic catalytic properties, good stability and circulation performance.

Related Products of 1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., 1575-37-7.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Electric Literature of 1575-37-7.

Gawandi, Sinthiya J.;Desai, Vidya G.;Joshi, Shrinivas;Shingade, Sunil;Pissurlenkar, Raghuvir R. research published ã€?Assessment of elementary derivatives of 1,5-benzodiazepine as anticancer agents with synergy potentialã€? the research content is summarized as follows. Herein, we designed and synthesized 1,5-benzodiazepines as a lead mol. for anticancer activity and as potent synergistic activity with drug Methotrexate. Working under the framework of green chem. principles, series of 1,5-benzodiazepine derivatives (3a-3a1) were synthesized using biocatalyst i.e. thiamine hydrochloride under solvent free neat heat conditions. These compounds were screened for in vitro anti cancer activity against couple of cancer cell lines (HeLa and HEPG2) and normal human cell line HEK-293 via MTT assay. Compound 3x was found to be influential against both the cell lines with IC50 values of 0.067 ± 0.002 μM against HeLa and 0.087 ± 0.003 μM against HEPG2 cell line, having activity as compatible to the standard drug Methotrexate. Bioinformatic anal. showed that these compounds are good tyrosine kinase inhibitors which was then proved using enzyme inhibition assay. The studies of apoptosis revealed late apoptotic mode of cell death for the compounds against HEPG2 cancer cell line using flow cytometry method. Synergistic studies of compound 3x and drug Methotrexate showed that the combination was highly active against cancer HeLa and HEPG2 cell line with IC50 value 0.046 ± 0.002 μM and 0.057 ± 0.002 μM resp., which was well supported by apoptosis pathway. Further the compounds proved its scope as DNA intercalating agents, as its mol. docking and DNA binding studies revealed that the compounds would fit well into the DNA strands.

1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., Electric Literature of 1575-37-7

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Category: bromides-buliding-blocks.

Ge, Yuxi;Huang, Bin research published ã€?Light-emitting analogues based on triphenylamine modified quinoxaline and pyridine[2,3-b]pyrazine exhibiting different mechanochromic luminescenceã€? the research content is summarized as follows. A series of light-emitting analogs, [4-(2,3-diphenyl-quinoxalin-6-yl)-phenyl]-diphenyl-amine (TPA-DPQ) and [4-(2,3-diphenyl-pyrido[2,3-b]pyrazin-7-yl)-phenyl]-diphenyl-amine (TPA-DPP) are synthesized and characterized. TPA-DPQ and TPA-DPP possess similar donor-acceptor structures, in which triphenylamine is used as an electron donor while 2,3-diphenyl-quinoxaline (DPQ) and its analog 2,3-diphenyl-pyridine[2,3-b]pyrazine (DPP) serve as electron acceptors. Due to the stronger electron-withdrawing ability of DPP compared with DPQ, TPA-DPP exhibits longer but weaker emission than TPA-DPQ as expected. However, TPA-DPQ and TPA-DPP show different mechanochromic luminescence (MCL) properties with emission color changes of 42 and 10 nm, resp. Crystallog. anal. demonstrates that changes of CH···π and CH···N intermol. interactions are responsible for the significantly different MCL behaviors of the two compounds This work will provide some guidance for the rational design of MCL-active fluorophores.

Category: bromides-buliding-blocks, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., 1575-37-7.

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. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine, Recommanded Product: 4-Bromobenzene-1,2-diamine

Fischer, Christian;Veprek, Nynke A.;Peitsinis, Zisis;Ruhmann, Klaus-Peter;Yang, Chao;Spradlin, Jessica N.;Dovala, Dustin;Nomura, Daniel K.;Zhang, Yingkai;Trauner, Dirk research published �De novo Design of SARS-CoV-2 Main Protease Inhibitors� the research content is summarized as follows. The COVID-19 pandemic prompted many scientists to investigate remedies against SARS-CoV-2 and related viruses that are likely to appear in the future. As the main protease of the virus, M ^Pro, is highly conserved among coronaviruses, it has emerged as a prime target for developing inhibitors. Using a combination of virtual screening and mol. modeling, we identified small mols. that were easily accessible and could be quickly diversified. Biochem. assays confirmed a class of pyridones as low micromolar noncovalent inhibitors of the viral main protease.

Recommanded Product: 4-Bromobenzene-1,2-diamine, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., 1575-37-7.

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. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine, Formula: C6H7BrN2

Fu, Jiaxu;Yan, Liuqing;Wang, Shuang;Song, Hongying;Gu, Qiang;Zhang, Yumin research published ã€?Microwave-assisted synthesis and luminescent properties of triphenylamine substituted mono- and di- branched benzimidazole derivativesã€? the research content is summarized as follows. In the present work, the synthesis of (benzoimidazolyl)-N,N-diphenylanilines I [R = H, Cl, Br, Me, CO₂H] and II using sodium metasulfite (Na₂S₂O₅) and p-toluenesulfonic acid (PTSA) sep. as catalysts was studied. Herein, the liquid phase microwave method was chosen to synthesize triphenylamine substituted mono- and di-branched benzimidazole derivatives compared with the solid phase microwave method, and the reaction conditions were optimized using Na₂S₂O₅ as a catalyst in N,N-dimethylformamide (DMF) solvent. A possible reaction mechanism was discussed. On this basis, PTSA using a catalyst was introduced into the reaction, the yields of the target products were evidently increased (the yield was enhanced 5-22% using PTSA as a catalyst). It is found that PTSA only acted as a catalyst, while Na₂S₂O₅ acted as both a catalyst and an oxidant, and PTSA could effectively catalyze the synthesis of benzimidazoles. Further, the luminescent properties of the synthesized compounds were comparatively studied after the structures of the synthesized compounds were confirmed. The results showed that the fluorescence quantum yield and the intensity of the synthesized compounds were enhanced with the increase in the number of substituted benzimidazole on triphenylamine, and the different substituents on 5-position of benzimidazole also had significant effect on the luminescent properties of the compound

1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., Formula: C6H7BrN2

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. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine, Quality Control of 1575-37-7

Fasiuddin, G. S.;Liakath Ali Khan, F.;Sakthivel, S.;Muthu, S.;Irfan, Ahmad research published ã€?Synthesis, Spectroscopic, Molecular Docking and inhibitory activity of 6-Bromo-2-(4-chlorophenyl)-1H-benzimidazole- a DFT approachã€? the research content is summarized as follows. A novel compound 6-bromo-2-(4-chlorophenyl)-1H-benzimidazole was synthesized to treat antimicrobial infections and characterized by FT-IR, FT-Raman, 1H-NMR, UV-Vis. The stable conformer and structural optimization were carried out using the DFT-B3LYP (6-311 ++ G (d, p)) method in Gaussian 16 W. FT-IR and FT-Raman exptl. and theor. wavenumbers with the complete vibrational assignment were reported. NMR of 1H -13C and UV-Vis is calculated at different solvents using the IEF-PCM method. The conductivity, reactivity and stability of the title compound are determined by HOMO-LUMO values. The antibacterial activity was tested against S. aureus and A. niger to indicate a significant zone of inhibition than the reference drug ciprofloxacin at the concentration of 25μg/mL, and protein and ligand interaction site in docking was determined by MEP. Finally, the mol. docking between the title and the reference compound ligand with the A. niger / 3EQA was studied and compared the binding energy of the compound at the active sites.

1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., Quality Control of 1575-37-7

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Recommanded Product: 4-Bromobenzene-1,2-diamine.

Fayed, Eman a.;Ammar, Yousry a.;Saleh, Marwa a.;Bayoumi, Ashraf h.;Belal, Amany;Mehany, Ahmed b. m.;Ragab, Ahmed research published ã€?Design, synthesis, antiproliferative evaluation, and molecular docking study of new quinoxaline derivatives as apoptotic inducers and EGFR inhibitorsã€? the research content is summarized as follows. A new series of quinoxaline derivatives I (R = 6-Br, 6-Cl, 7-PhCO; X = MeO, H₂NNH) and II [R = H, 6-Br-6-Cl-7-PhCO; X = HO, MeO, EtO, H₂NNH, PhC(O)NHNH, 4-MeC₆H₄CH:NNH, etc.] were synthesized and pharmacol. evaluated against HepG-2, HCT-116, and MCF-7 cell lines. Seven compounds I (R = 6-Cl, 6-Br; X = H₂NNH), II (R = 6-Cl, 6-Br, 7-PhCO, X = MeO; R = 6-Cl, X = EtO) and 3,4-dihydro-2H-pyrano[2,3-b]quinoxalin-2-one were found to possess the highest activities against the examined cell lines with IC₅₀ values ranging from (7.57 to 28.44μM). These compounds were further selected to analyze their apoptotic potential in MCF-7 cells. Interestingly, it was found that the Bcl-2 level decreased by 1.95-3.99 times and the BAX level increased by 7.2-10.6 times relative to the control. These compounds also increased the active Caspase-3 level by 5.77-10.69 folds compared to untreated cells. WI-38 cells were treated with these compounds to estimate the cytotoxicity level of in non-tumorigenic cells, and these compounds displayed higher IC₅₀ values (142.21-335.03μM). Further studies on the mechanism of the most promising compounds I (R = 6-Br; X = H₂NNH), II (R = 6-Cl, 6-Br; X = MeO) and 3,4-dihydro-2H-pyrano[2,3-b]quinoxalin-2-one, revealed that they increase apoptotic cells and induce cell cycle arrest at pre-G1 and G2/M phases. Besides, evaluation of both wild EGFRWT and mutant EGFRL858R-TK inhibitory activity for these derivatives showed IC₅₀ values ranging from 0.075-1.547μM vs. wild EGFRWT and 63.70-87.34 nM vs. the mutant type. Erlotinib was used as a standard reference with IC₅₀ values of 0.0656μM and 59.56 nM vs. both types. Finally, the mol. docking study of most potent quinoxaline derivatives exhibited a good binding inside the active site of EGFR (1M17), with binding energy ranged between (-15.86 to -16.97) compared to Erlotinib (-17.84) kcal/mol. Also, by applying Lipinski’s parameters, it was found that these derivatives showed no violations and indicated possibility to formulate orally.

1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., Recommanded Product: 4-Bromobenzene-1,2-diamine

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 1575-37-7, formula is C6H7BrN2, The most pervasive is the naturally produced bromomethane. Electric Literature of 1575-37-7

Elumalai, Vijayaragavan;Hansen, Joern H. research published �A Green, Scalable, and Catalyst-Free One-Minute Synthesis of Quinoxalines� the research content is summarized as follows. A highly efficient and catalyst-free protocol was reported for the synthesis of quinoxalines via the classical cyclocondensation reaction between aryldiamines and dicarbonyl compounds Remarkably simple and green reaction conditions employed methanol as solvent afforded medium to excellent yield of quinoxalines after only one-minute reaction time at ambient temperature The conditions allow at least 10 g scale synthesis of quinoxalines and preferred starting point for optimization and method of choice for applications in the synthetic community.

1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., Electric Literature of 1575-37-7

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Reference of 1575-37-7.

Ding, Ling;Niu, Kaikai;Liu, Yuxiu;Wang, Qingmin research published �Electro-reductive C-H cyanoalkylation of quinoxalin-2(1H)-ones� the research content is summarized as follows. Herein, authors report a practical electro-reductive protocol for the direct C-H cyanoalkylation of quinoxalin-2(1H)-ones via iminyl radical-mediated ring opening. These mild reactions proceed under metal-, reductant-, and reagent-free conditions to provide synthetically useful cyanoalkylated quinoxalin-2(1H)-ones.

1575-37-7, 4-Bromo-1,2-diaminobenzene can be obtained from 1,2-diaminobenzene via acetylation followed by bromination and alkaline hydrolysis.
4-Bromobenzene-1,2-diamine, also known as 4-Bromobenzene-1,2-diamine, is a useful research compound. Its molecular formula is C6H7BrN2 and its molecular weight is 187.04 g/mol. The purity is usually 95%.
4-Bromo-1,2-diaminobenzene is a dye that is used in diagnostic
procedures to detect the presence of amide groups. 4-Bromo-1,2-diaminobenzene can be used as an inhibitor for cationic polymerization reactions. It also has tuberculostatic activity and inhibits the growth of Mycobacterium tuberculosis. This compound reacts with aniline to form a benzimidazole derivative that contains a reactive amine group. The reaction between this amine group and different electrophiles generates benzimidazole compounds with different properties that are useful in nucleophilic attack reactions. The reaction between 4-bromo-1,2-diaminobenzene and methyl ethyl sulfide produces a luminescent probe that can be used to detect hydrogen bonds., Reference of 1575-37-7

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary