Category: bromides-buliding-blocks

Organic compounds having carbon bonded to bromine are called organic bromides. 2576-47-8, formula is C2H7Br2N, Name is 2-Bromoethylamine hydrobromide. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. HPLC of Formula: 2576-47-8.

Tian, Dongjie;Lai, Zhiwei;Xu, Han;Lin, Fangyuan;Jiang, Yaqi;Huang, Yipeng;Wang, Shuya;Cai, Yuting;Jin, Jingwen;Xie, Rong-Jun;Chen, Xi research published 《 Low-Dimensional Organic Lead Halides with Organic-Inorganic Collaborative Luminescence Regulated by Anion in Dimension》, the research content is summarized as follows. Low-dimensional (LD) organic-metal halides (OMHs) have been extensively investigated because of their excellent optical properties. However, the rational synthetic control (dimension regulation) of LD-OMHs has not yet been established well. The effect of organic cations on the luminescence also remains unexplored. Here, we designed a double-chain ammonium salt 1 with two amine functional groups. Using hydrogen bonding between -N-H₃ protons and halogen ions synthesized zero-dimensional (0D) OMH C₁₂H₃₀N₄Pb₂Br₈ (2). Furthermore, through introducing other ionic interactions to regulate the dimension of OMHs, we obtained one-dimensional (1D) OMH C₁₂H₃₀N₄Pb₂Cl_7.5Br_0.5 (3) by anion exchange of 2. Through the in-depth anal. of their crystal structure, it is understood that the design of organic cations and the exchange of anions can regulate the dimension of OMHs through the change of hydrogen bonds in the structure. This sets a foundation for the formation of a synthesis mechanism for LD-OMHs and effective regulation of OMHs dimension. Through crystal structure anal., experiments, and theor. calculations, this work proves that the emission of 2 is not dominated by a single factor of organic cations or metal halogen octahedrons but by the interaction of organic cations and metal octahedrons. Moreover, the 1D-OMH 3 shows tunable emissions from blue to white light under varying excitation wavelengths, which provides a foundation for expanding the application of OMHs.

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

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. 20469-65-2, formula is C8H9BrO2, Name is 1-Bromo-3,5-dimethoxybenzene, Application of C8H9BrO2

Tian, Xianhai;Kaur, Jaspreet;Yakubov, Shahboz;Barham, Joshua P. research published 《 α-Amino Radical Halogen Atom Transfer Agents for Metallaphotoredox-Catalyzed Cross-Electrophile Couplings of Distinct Organic Halides》, the research content is summarized as follows. α-Amino radicals from simple tertiary amines were employed as halogen atom transfer (XAT) agents in metallaphotoredox catalysis for cross-electrophile couplings of organic bromides with organic iodides. This XAT strategy proved to be efficient for the generation of carbon radicals from a range of partners (alkyl, aryl, alkenyl, and alkynyl iodides). The reactivities of these radical intermediates were captured by nickel catalysis with organobromides including aryl, heteroaryl, alkenyl, and alkyl bromides, enabling six diverse C-C bond formations. Classic named reactions including Negishi, Suzuki, Heck, and Sonogashira reactions were readily achieved in a net-reductive fashion under mild conditions. More importantly, the cross coupling was viable with either organic bromide or iodide as limiting reactant based on the availability of substrates, which is beneficial to the late-stage functionalization of complex mols. The scalability of this method in batch and flow was investigated, further demonstrating its applicability.

Application of C8H9BrO2, 1-Bromo-3,5-dimethoxybenzene, also known as 1-Bromo-3,5-dimethoxybenzene, is a useful research compound. Its molecular formula is C8H9BrO2 and its molecular weight is 217.06 g/mol. The purity is usually 95%.
1-Bromo-3,5-dimethoxybenzene is used as an intermediate in the synthetic preparation of pharmaceutical inhibitors via cross-coupling reactions.
1-Bromo-3,5-dimethoxybenzene can be synthesized by using 1,3-dimethoxybenzene via iridium-catalyzed arene borylation.
1-Bromo-3,5-dimethoxybenzene (1BDMB) is a synthetic molecule that can be used as an electron acceptor in organic photovoltaic cells. 1BDMB is a salt of the sodium salt of resorcylic acid and 1,3-dibromo-5,5-dimethoxybenzene. It has been shown to have a radical mechanism for the generation of free radicals. The radical mechanism is initiated by light absorption by the ruthenium complex at the center of the molecule which induces photoinduced electron transfer from the ruthenium to 1BDMB. This process results in electron transfer from the donor to an acceptor molecule, such as oxygen or nitrogen. The pharmacokinetic properties of this compound are not well known; however, it has been demonstrated that it can be synthesized through a cross-coupling reaction with other aromatic compounds such as stemofuran., 20469-65-2.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic compounds having carbon bonded to bromine are called organic bromides. 823-78-9, formula is C7H6Br2, Name is 1-Bromo-3-(bromomethyl)benzene. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Product Details of C7H6Br2.

Tian, Xue-Rong;Peng, Xing-Jie;Zhao, Tong-Tong;Bian, Qiang;Zhao, Wei-Guang research published 《 Design, synthesis, and fungicidal activities of novel ethylenediamine bridged thiazole derivatives containing oxime ether or oxime ester moieties》, the research content is summarized as follows. To study the influence of changing the piperidine ring on the fungicidal activity, at the same time based on the successful experience of opening the oxazoline ring, a series of novel ethylenediamine bridged thiazole derivatives containing oxime ether and oxime ester moieties I (R = Me, Et; R¹ = Bn, 4-MeC₆H₄CH₂, 2-ClC₆H₄CH₂, etc.), II (R = Me; R² = Ph, 2-FC₆H₄, 4-ClC₆H₄, etc.) and III (R = n-Pr, n-Bu, Bn) were designed, synthesized, and first evaluated for their fungicidal activities against phytophthora capsici in vitro. The bioassays results showed that the target compounds possessed moderate fungicidal activities against phytophthora capsici. Compound III (R = n-Bu) showed 53.6% fungicidal activity at 50 μg/mL. Oxime ether and oxime ester derivatives showed the similar level of activities. However, the activities of these compounds were lower than that of oxathiapiprolin, suggesting the piperidine ring was essential to maintain the fungicidal activities of these compounds For the oxime ether derivatives, I (R = Me, Et; R¹ = 2-MeC₆H₄CH₂), III (R = n-Pr, n-Bu) the substituents on ethylenediamine have certain influence on the activity. Increasing the chain length of substituents is beneficial to the fungicidal activity. Meanwhile, these compounds were tested their fungicidal activities against other 9 fungi, and these compounds showed broad spectrum fungicidal activities. Some compounds exhibited more than 70% fungicial activities against specific fungi.

Product Details of C7H6Br2, 3-Bromobenzyl bromide undergoes reduction with diethylzinc in the presence of Pd(PPh3)4 to yield corresponding hydrocarbon.

3-Bromobenzyl bromide is a useful research compound. Its molecular formula is C7H6Br2 and its molecular weight is 249.93 g/mol. The purity is usually 95%.

3-Bromobenzyl bromide is a molecule that has been synthesized and shown to have anticancer activity. It inhibits the activity of cancer cells by binding to amines in these cells and preventing the formation of hydrogen bonds between these molecules. 3-Bromobenzyl bromide has also been shown to selectively inhibit the activity of NS5B polymerase, an enzyme that is important in the replication of the hepatitis C virus. The synthetic nature of this molecule makes it an attractive target for analytical methods such as nuclear magnetic resonance spectroscopy. This molecule also shows significant cytotoxicity against cancer cell lines in vitro, as well as inducing tumor necrosis factor-alpha (TNF-α) production in lps-stimulated murine macrophages., 823-78-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 4224-70-8, formula is C6H11BrO2, Name is 6-Bromohexanoic acid. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Synthetic Route of 4224-70-8.

Tian, Yiqiang;Liu, Xiaojie;He, Bangyue;Ren, Yuxi;Su, Weiping research published 《 A facile method for Rh-catalyzed decarbonylative ortho-C-H alkylation of (hetero)arenes with alkyl carboxylic acids》, the research content is summarized as follows. A facile and effective method for Rh-catalyzed direct ortho-alkylation of C-H bonds in (hetero)arenes I (R = 2-methylphenyl, naphthalen-1-yl, thiophen-2-yl, etc.) with com. available carboxylic acids R¹COOH (R¹ = Et, cyclopentyl, 2-(4-bromophenyl)ethyl, etc.) has been developed. This strategy was initiated by in situ conversion of carboxylic acids to anhydrides which, without isolation, underwent Rh-catalyzed direct decarbonylative cross-coupling of aryl carboxamides containing 8-aminoquinoline I (R = 2,6-diethylphenyl, 2-cyclopentyl-6-methylphenyl, 2-methyl-6-phenylphenyl, etc.). The reaction proceeds with high regioselectivity and exhibits a broad substrate scope as well as functional group tolerance.

4224-70-8, 6-bromohexanoic acid is an organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. It derives from a hexanoic acid.
6-Bromohexanoic acid is a useful research compound. Its molecular formula is C6H11BrO2 and its molecular weight is 195.05 g/mol. The purity is usually 95%.
6-Bromohexanoic acid is useful for the preparation of anti-CTLA4 compounds as antitumor agents.
6-Bromohexanoic acid is a fatty acid that has been shown to be an effective agent for the treatment of cancer. It is used in gene therapy to inhibit the growth of cancer cells by binding to and then activating transcription factors. 6-Bromohexanoic acid can also be used as a chemotherapeutic agent and has been shown to cause apoptosis in monoclonal antibody-treated cells. 6-Bromohexanoic acid has pharmacokinetic properties that are similar to those of other fatty acids. The reaction solution was found to have high chemical stability, which may be due to the presence of nitrogen atoms. This reaction solution was found to adsorb onto the surface of monoclonal antibodies and cell culture, altering their properties., Synthetic Route of 4224-70-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 402-49-3, formula is C8H6BrF3, Name is 1-(Bromomethyl)-4-(trifluoromethyl)benzene. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. Recommanded Product: 1-(Bromomethyl)-4-(trifluoromethyl)benzene.

Szczesniak, Piotr;Furman, Bartlomiej research published 《 Photo-Fries-type rearrangement of cyclic enamides. An efficient route to structurally diverse five-membered enaminones》, the research content is summarized as follows. A simple, efficient and user-friendly protocol for the preparation of structurally diverse enaminones e.g., I from enamides e.g., II has been developed. The strategy is based on a photo-induced intramol. Fries-type rearrangement. The photochem. transformation proceeds under mild reaction conditions, applies to a broad substrate range, is highly economic, and limits the amount of waste produced. The proposed methodol. was used as a key step in the synthesis of dihydrojasmone an important fragrance compound

402-49-3, 4-Trifluoromethylbenzyl bromide is a useful research compound. Its molecular formula is C8H6BrF3 and its molecular weight is 239.03 g/mol. The purity is usually 95%.
4-Trifluoromethylbenzyl bromide is a choline derivative that acts as an anticancer agent. It is structurally similar to the anticancer drug doxorubicin, which has been shown to be effective against breast cancer and leukemia. 4-Trifluoromethylbenzyl bromide interacts with cellular proteins, including choline kinase, and inhibits the mitochondrial pathway. This leads to cell death through apoptosis. The molecule also interacts with nucleotide bases such as thymine and cytosine in DNA, inhibiting transcription and replication. 4-Trifluoromethylbenzyl bromide binds strongly to the hydroxyl group of cholesterol by an electrophilic substitution mechanism to form a covalent bond with its hydroxy group. The molecule can also bind to chloride ions by an ionic bond., Recommanded Product: 1-(Bromomethyl)-4-(trifluoromethyl)benzene

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic compounds having carbon bonded to bromine are called organic bromides. 6911-87-1, formula is C7H8BrN, Name is 4-Bromo-N-methylaniline. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Recommanded Product: 4-Bromo-N-methylaniline.

Szymor-Pietrzak, Damian;Khan, Muhammad N.;Pages, Anais;Kumar, Ajay;Depner, Noah;Clive, Derrick L. J. research published 《 Formation of 3-Aminophenols from Cyclohexane-1,3-diones》, the research content is summarized as follows. Meta-Aminophenols are formed by the action of DBU on 3-amino-2-chlorocyclohex-2-en-1-ones at room temperature in MeCN. The chloro compounds are generated by treating 3-aminocyclohex-2-en-1-ones with the easily prepared halogenating agent BnNMe3·ICl2 in MeOH-CH2Cl2. The amino group must carry two substituents, either two aryl, one aryl and one alkyl, or two alkyl groups; 3-aminocyclohex-2-en-1-ones of this type are readily made from cyclohex-2-en-1-one and a primary or secondary amine.

6911-87-1, 4-Bromo-N-methylaniline is a aniline based compound known to exhibit mutagenic properties.
4-Bromo-N-methylaniline is a useful research compound. Its molecular formula is C7H8BrN and its molecular weight is 186.05 g/mol. The purity is usually 95%.
4-Bromophenylmethylamine is an organic compound that has anti-inflammatory properties and is used as a pharmaceutical. It belongs to the group of amines. The hydrolysis of 4-bromophenylmethylamine by hydrochloric acid produces phenol and bromamine (NHBr). The reaction system can be used to synthesize a number of compounds, including anilines, benzofurans, and other aromatic compounds. 4-Bromophenylmethylamine reacts with muscle tissue in a similar manner as acetaminophen does. This drug also has been shown to have significant effects on the energy metabolism in the muscles of rats that are given carbon source., Recommanded Product: 4-Bromo-N-methylaniline

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 70-23-5, formula is C5H7BrO3, Name is Ethyl 3-bromo-2-oxopropanoate. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Computed Properties of 70-23-5.

Tabarsaei, Navisa;Hamedani, Naghmeh Faal;Shafiee, Shahin;Khandan, Samira;Hossaini, Zinatossadat research published 《 Catalyst-free green synthesis and study of antioxidant activity of new pyrazole derivatives》, the research content is summarized as follows. In this research, a novel procedure for the synthesis of pyrazole derivatives in excellent yields was studied using catalyst-free multicomponent reaction of isoquinoline, activated acetylenic compounds, alkyl bromides, triphenylphosphine and hydrazine in water under ultrasonic irradiation at room temperature The advantages of this procedure than to reported methods are short time of reaction, high yields of product, easy separation of product, clean mixture of reaction and green media for performing reaction. In addition, because of having pyrazole and isoquinoline core in the synthesized compounds, in this research, antioxidant activity of some synthesized compounds was investigated.

70-23-5, Ethyl bromopyruvate molecular formula is C5H7BrO3 and its molecular weight is 195.01 g/mol. The purity is usually 95%.

Ethyl bromopyruvate is used in a synthesis of thioxothiazolidines from carbon disulfide and primary amines.

Ethyl bromopyruvate is a chemical inhibitor that inhibits the enzyme pyruvate dehydrogenase, which is responsible for the conversion of pyruvic acid to acetyl-CoA. This inhibition leads to a decrease in ATP levels and can cause metabolic disorders. Ethyl bromopyruvate is used as an anthelmintic drug and in asymmetric synthesis. It is also used in the synthesis of thiostrepton, an antibiotic that has been shown to have antimicrobial activity against Gram-positive bacteria, including Staphylococcus aureus and Streptococcus pneumoniae., Computed Properties of 70-23-5

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 4897-84-1, formula is C5H9BrO2, Name is Methyl 4-bromobutanoate. Organic compounds having carbon bonded to bromine are called organic bromides. Recommanded Product: Methyl 4-bromobutanoate.

Tabata, Hidetsugu;Murai, Kazuya;Funaki, Kaoru;Takemae, Chihiro;Tasaka, Tomohiko;Oshitari, Tetsuta;Takahashi, Hideyo;Natsugari, Hideaki research published 《 Atropisomeric and conformational properties of 6N-benzoyl- and 6N-p-tosyl-1,6-benzodiazocines: comparison with those of 1,5-benzodiazepines》, the research content is summarized as follows. The atropisomeric and conformational properties of the eight-membered 1,6-benzodiazocines (2) with 6N-benzoyl (A) and 6N-p-tosyl (B) groups were examined by comparing them with those of the seven-membered 1,5-benzodiazepine congeners (1) (A, B). The conformation (orientation) of the benzene ring in the benzoyl and tosyl groups differed depending on the ring size (7/8) and N-substituent (-CO-/-SO₂-). The activation free-energy barrier to rotation of the axes in N-p-tosyl derivatives (B) was shown to be much higher than those of the benzoyl derivatives (A).

4897-84-1, Methyl 4-bromobutyrate,also as known as 4-Bromobutyric acid methyl ester, is a useful research compound. Its molecular formula is C5H9BrO2 and its molecular weight is 181.03 g/mol. The purity is usually 95%.
4-Bromobutyric acid methyl ester is a synthetic compound that can be used to inhibit the activity of the G1 phase cyclin-dependent kinases. It has been shown to inhibit protein synthesis by alkylating the amino groups of proteins and fatty acids. 4-Bromobutyric acid methyl ester also inhibits the growth of cancer cell lines, such as renal carcinoma cells. The mechanism of action for this drug is not well understood, but it may be due to its ability to bind with monoclonal antibodies and enter kidney cells by passive diffusion., Recommanded Product: Methyl 4-bromobutanoate

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 4224-70-8, formula is C6H11BrO2, Name is 6-Bromohexanoic acid. Organic compounds having carbon bonded to bromine are called organic bromides. Reference of 4224-70-8.

Tahir, M. Nazir;Harati, Masoud;Nyayachavadi, Audithya;Rezapour, Mehdi;Eichhorn, S. Holger;Rondeau-Gagne, Simon research published 《 Intrinsically Porous Polydiacetylene from a Functionalized Bowl-Shaped Hexaphenoxycyclotriphosphazene Derivative》, the research content is summarized as follows. Intrinsic porosity in polymeric materials arises from the formation of a continuous network of interconnected voids and is a direct consequence of the shape and rigidity of the mol. building blocks. To obtain well-defined pores with narrow size distributions, the polymerization of rigid and sterically hindered monomers must not interfere with the pore formation and should avoid the use of additives that may occupy voids. Polydiacetylenes can be generated by the topochem. polymerization of diacetylene-bearing mols. favorably arranged in crystals, gels, thin films, or vesicles. Polydiacetylene formation in amorphous materials has been sparsely studied because higher-order self-assembled structures are assumed to be required for the topochem. polymerization of 1,3-butadiyne to occur. In this study, a bulky hexachlorocyclotriphosphazene core (N₃P₃Cl₆) was functionalized with six diacetylene-containing alkyl chains and successfully converted to an intrinsically porous multifunctional polydiacetylene. The successful formation of the polydiacetylene was confirmed by Raman spectroscopy, and the porous structure of the resulting materials was verified by X-ray diffraction and Brunauer-Emmett-Teller surface area measurements. This investigation revealed a significant change in the porous structure after polymerization, leading to a 5-fold increase in sp. surface area. Overall, the topochem. polymerization of diacetylenes is a promising strategy for the preparation of functional materials, which is shown to be compatible with rather amorphous phases of bulky mols. The results obtained from this investigation give access to a range of porous polydiacetylene materials for potential applications in organic electronics, gas adsorption, and other related fields.

4224-70-8, 6-bromohexanoic acid is an organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. It derives from a hexanoic acid.
6-Bromohexanoic acid is a useful research compound. Its molecular formula is C6H11BrO2 and its molecular weight is 195.05 g/mol. The purity is usually 95%.
6-Bromohexanoic acid is useful for the preparation of anti-CTLA4 compounds as antitumor agents.
6-Bromohexanoic acid is a fatty acid that has been shown to be an effective agent for the treatment of cancer. It is used in gene therapy to inhibit the growth of cancer cells by binding to and then activating transcription factors. 6-Bromohexanoic acid can also be used as a chemotherapeutic agent and has been shown to cause apoptosis in monoclonal antibody-treated cells. 6-Bromohexanoic acid has pharmacokinetic properties that are similar to those of other fatty acids. The reaction solution was found to have high chemical stability, which may be due to the presence of nitrogen atoms. This reaction solution was found to adsorb onto the surface of monoclonal antibodies and cell culture, altering their properties., Reference of 4224-70-8

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic compounds having carbon bonded to bromine are called organic bromides. 823-78-9, formula is C7H6Br2, Name is 1-Bromo-3-(bromomethyl)benzene. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Reference of 823-78-9.

Tan, Hui;Wang, Shen-An;Yan, Zixi;Liu, Jianzhong;Wei, Jialiang;Song, Song;Jiao, Ning research published 《 N-Heterocyclic Carbene Catalyzed Ester Synthesis from Organic Halides through Incorporation of Oxygen Atoms from Air》, the research content is summarized as follows. Oxygenation reactions with mol. oxygen (O₂) as the oxygen source provides a green and straightforward strategy for the construction of O-containing compounds Demonstrated here is a novel N-heterocyclic carbene (NHC) catalyzed oxidative transformation of simple and readily available organic halides into valuable esters through the incorporation of O-atoms from O₂. Mechanistic studies prove that the deoxy Breslow intermediate generated in situ is oxidized to a Breslow intermediate for further transformation by this oxidative protocol. This method broadens the field of NHC catalysis and promotes oxygenation reactions with O₂.

823-78-9, 3-Bromobenzyl bromide undergoes reduction with diethylzinc in the presence of Pd(PPh3)4 to yield corresponding hydrocarbon.

3-Bromobenzyl bromide is a useful research compound. Its molecular formula is C7H6Br2 and its molecular weight is 249.93 g/mol. The purity is usually 95%.

3-Bromobenzyl bromide is a molecule that has been synthesized and shown to have anticancer activity. It inhibits the activity of cancer cells by binding to amines in these cells and preventing the formation of hydrogen bonds between these molecules. 3-Bromobenzyl bromide has also been shown to selectively inhibit the activity of NS5B polymerase, an enzyme that is important in the replication of the hepatitis C virus. The synthetic nature of this molecule makes it an attractive target for analytical methods such as nuclear magnetic resonance spectroscopy. This molecule also shows significant cytotoxicity against cancer cell lines in vitro, as well as inducing tumor necrosis factor-alpha (TNF-α) production in lps-stimulated murine macrophages., Reference of 823-78-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary