Zhu, Xiaolong team published research in Organic Chemistry Frontiers in 2022 | 1575-37-7

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.

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 1575-37-7, formula is C6H7BrN2, Name is 4-Bromobenzene-1,2-diamine. Organic compounds having carbon bonded to bromine are called organic bromides. Recommanded Product: 4-Bromobenzene-1,2-diamine.

Zhu, Xiaolong;Jiang, Min;Li, Xuan;Zhu, Enjie;Deng, Qirong;Song, Xiuyan;Lv, Jian;Yang, Daoshan research published 《 Alkylsulfonium salts for the photochemical desulfurative functionalization of heteroarenes》, the research content is summarized as follows. An efficient, metal-free organic photoredox-catalyzed direct alkylation of heteroarenes ArH (Ar = N-methyl-2-oxoquinoxalin-3-yl, 3,6-dichloropyridazin-4-yl, 2-oxoquinoxalin-3-yl, etc.) via a desulfurization strategy using alkylsulfonium salts I (R = Ph, 1-naphthyl, 2-thienyl, etc.; R1 = H, Me; X = PF6, BF4) as alkylation reagents under mild conditions has been described for the first time. The inexpensive and efficient organic photoredox-catalyzed method offers a new and useful strategy for constructing various biol. interesting heteroarenes ArCHRR1 in the fields of synthetic and pharmaceutical chem., and extends the scope of the still limited sulfonium salt photochem.

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