Kong, Xianqiang team published research in Asian Journal of Organic Chemistry in 2020 | 2905-24-0

Electric Literature of 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., 2905-24-0.

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. Electric Literature of 2905-24-0.

Kong, Xianqiang;Yu, Ke;Chen, Qianjin;Xu, Bo research published ã€?Electrochemical Oxidation-induced Difunctionalization of Alkynes and Alkenes with Sulfonyl Hydrazides: Facile Access to β-Selenovinyl Sulfones and β-Ketosulfonesã€? the research content is summarized as follows. Herein, an efficient electrochem. oxidative selenosulfonylation of alkynes R1CCR2 (R1 = Et, Ph, naphthalen-2-yl, etc.; R2 = H, Me, Ph, etc.) and oxysulfonylation of alkenes R3CH=CH2 (R3 = H, 4-nitrophenyl, 3,4-dichlorophenyl, etc.) without use of metal catalysts were reported. This method provides a practical access to a wide range of β-(seleno)vinyl sulfones RS(O)2C(R2)=C(R1)SePh (R = Et, 4-chlorophenyl, thiophen-2-yl, etc.) and β-keto sulfones RS(O)2CH2C(O)R3. These reactions can tolerate various functional groups and be easily scaled-up.

Electric Literature of 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., 2905-24-0.

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