Yang, Chang-Jiang team published research in Nature Catalysis in 2020 | 2905-24-0

2905-24-0, 3-Bromobenzenesulfonyl chloride is an aryl sulfonyl chloride derivative. It participates in the synthesis of N-sulfonylanthranilic acid derivatives and potent P1′ benzenesulfonyl azacyclic urea human immunodeficiency virus (HIV) protease inhibitors.
3-Bromobenzenesulfonyl chloride is a molecule that can be used to inhibit the uptake of 3-bromobenzoate. The inhibition of uptake is due to the desymmetrization of the unsymmetrical, 3-bromobenzoate. This reaction leads to an increase in the concentration of 3-bromobenzoate. Inhibition studies have shown that 3-bromobenzenesulfonyl chloride has an inhibitory effect on cancer cells and apoptosis pathway. The structural studies have shown that this drug is synthetic and biphenyl can be synthesized from it. T-cell lymphomas have been shown to be inhibited by this drug and heart disease has also been inhibited., Recommanded Product: 3-Bromobenzenesulfonyl chloride

Chloride substituents modify the physical properties of organic compounds in several ways. 2905-24-0, formula is C6H4BrClO2S, Name is 3-Bromobenzenesulfonyl chloride. They are typically denser than water due to the presence of chlorine, which has a high atomic weight. Recommanded Product: 3-Bromobenzenesulfonyl chloride.

Yang, Chang-Jiang;Zhang, Chi;Gu, Qiang-Shuai;Fang, Jia-Heng;Su, Xiao-Long;Ye, Liu;Sun, Yan;Tian, Yu;Li, Zhong-Liang;Liu, Xin-Yuan research published 《 Cu-Catalysed intramolecular radical enantioconvergent tertiary β-C(sp3)-H amination of racemic ketones》, the research content is summarized as follows. Herein, the combination of decoupled hydrogen atom abstraction with asym. copper catalysis for enantioconvergent tertiary β-C(sp3)-H amination of racemic ketones was described. This method, when allied with follow-up transformations, provided facile access to a range of enantioenriched compounds I [R = t-Bu, Ph, 3-thienyl, etc.; R1 = Me, CH2CO2Me, allyl, etc.; R2 = Ph, 2-thienyl, 3-thienyl, 3-MeC6H4; Ar = Ph, 4-tolyl, 2-naphthyl, etc.] featuring quaternary stereocenters.

2905-24-0, 3-Bromobenzenesulfonyl chloride is an aryl sulfonyl chloride derivative. It participates in the synthesis of N-sulfonylanthranilic acid derivatives and potent P1′ benzenesulfonyl azacyclic urea human immunodeficiency virus (HIV) protease inhibitors.
3-Bromobenzenesulfonyl chloride is a molecule that can be used to inhibit the uptake of 3-bromobenzoate. The inhibition of uptake is due to the desymmetrization of the unsymmetrical, 3-bromobenzoate. This reaction leads to an increase in the concentration of 3-bromobenzoate. Inhibition studies have shown that 3-bromobenzenesulfonyl chloride has an inhibitory effect on cancer cells and apoptosis pathway. The structural studies have shown that this drug is synthetic and biphenyl can be synthesized from it. T-cell lymphomas have been shown to be inhibited by this drug and heart disease has also been inhibited., Recommanded Product: 3-Bromobenzenesulfonyl chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics