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.
Vasu, Amrutham;Naresh, Mameda;Krishna Sai, Gajula;Divya Rohini, Yennamaneni;Murali, Boosa;Ramulamma, Madasu;Ramunaidu, Addipilli;Narender, Nama research published 《 A heterogeneous catalytic strategy for facile production of benzimidazoles and quinoxalines from primary amines using the Al-MCM-41 catalyst》, the research content is summarized as follows. This study reported a straightforward heterogeneous catalytic (Al-MCM-41) approach to synthesize benzimidazoles I [R = n-Pr, cyclohexyl, Ph, etc.; R1 = H, 5-Me, 5,6-di-Cl, etc.; R2 = H, Bn, CH2CH2Ph] and quinoxalines II [R3 = H, 6-Me, 6-Br, etc.; R4 = H, 4-MeC6H4, 4-ClC6H4, etc.] from primary amines under solvent-free conditions. The Al-MCM-41 catalyst was prepared using a hydrothermal method and characterized by various anal. techniques. The probability and limitations of the catalytic methodol. were presented with various substrates. The catalytic method grants an attractive route to a wide variety of benzimidazole and quinoxaline moieties with good to excellent yields. The gram scale reaction and reusability (up to five cycles) of the Al-MCM-41 catalyst would greatly benefit industrial applications.
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., Related Products of 1575-37-7
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary