Wen, Tiantian team published research in Materials Chemistry and Physics in 2022 | 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., Reference of 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. Reference of 1575-37-7.

Wen, Tiantian;Wang, Mingliang;Gao, Jie;Wang, Lanzhi research published 《 Cerium-enriched magnetic/recyclable dual-acid nanocatalyst for one-pot three-component synthesis of functionalized 1,5-benzodiazepines》, the research content is summarized as follows. Cerium enriched magnetic dual-acid nanocatalyst (CoFe2O4@SiO2@APTES@ATA-CeCl3) as green and recoverable nanocatalyst was prepared The novel nanocatalyst was characterized by Fourier transform IR spectroscopy (FT-IR), powder X-ray diffraction (XRD), SEM, energy-dispersive X-ray spectroscopy (EDS), inductively coupled plasma at. emission spectrometry (ICP-AES), transmission electron microscopy (TEM), XPS, nitrogen absorption-desorption experiment, and vibrating sample magnetometer (VSM). The dual-acid nanocatalyst was able to efficiently catalyze the synthesis of functionalized 1,5-benzodiazepines following through a three-component domino reaction of various substituted o-phenylenediamine, 1,3-dicarbonyl compounds, and phenylacetaldehyde. The dual-acid sites of Bronsted acid (2-aminoterephthalic acid (ATA)) and Lewis acid (CeCl3) of the catalysts were determinant features. Furthermore, a plausible catalytic mechanism had been proposed. The dual-acid nanocatalyst could be simply separated and reused without any remarkable decrease within the yield after six runs.

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