An, Xiaoying team published research on Hebei Shifan Daxue Xuebao, Ziran Kexueban in 2021 | 1575-37-7

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., Application of C6H7BrN2

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. Application of C6H7BrN2.

An, Xiaoying;Bai, Fan;Li, Wenhong;Wang, Lanzhi research published 《 Synthesis of 2,3-diester-2,4-diphenyl-1,5-benzodiazepine compounds via one-pot three-component tandem reactions》, the research content is summarized as follows. In this paper, seven novel 2,3-diester-2,4-diphenyl-1,5-benzodiazepines with imine structure were obtained via one-pot three-component tandem reactions catalyzed by TsOH in ethanol. With substituted 1,2-phenylenediamines, Et benzoylacetate and Et benzoylformate as the raw materials, the tandem reactions undergo two nucleophilic addition-dehydration processes to form the active intermediate mols. containing imine and enamine structures, further undergo carbon-carbon coupling cyclization and hydrogen transfer to yield the target products. A reasonable reaction mechanism is proposed for this three-component tandem reaction. The synthesis has the advantages of environmental friendliness, mild reaction conditions, wide substrate range, etc., which provides a green, efficient and convenient synthetic route for nitrogen-containing heterocyclic compounds

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., Application of C6H7BrN2

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary