Yu, Mingming team published research in Cell Reports Physical Science in 2021 | 2905-24-0

Category: chlorides-buliding-blocks, 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.

The class of organic compounds having covalently a bonded chlorine atom is called organic chlorides. 2905-24-0, formula is C6H4BrClO2S, Name is 3-Bromobenzenesulfonyl chloride. Their wide structural variety and divergent chemical properties lead to a broad range of named reactions and applications. Category: chlorides-buliding-blocks.

Yu, Mingming;Wang, Huamin;Gao, Yuhan;Bu, Faxiang;Cong, Hengjiang;Lei, Aiwen research published 《 Manganese-catalyzed chlorosulfonylation of terminal alkene and alkyne via convergent paired electrolysis》, the research content is summarized as follows. A manganese-catalyzed, atom-transfer radical addition of the terminal aryl alkenes ArCH=CH2 (Ar = Ph, 4-chlorophenyl, 4-(acetyloxy)benzen-1-yl, etc.) and alkynes ArCCH with sulfonyl chlorides RS(O)2Cl (R = 4-methylphenyl, naphthalen-1-yl, 1-methyl-1H-pyrazol-3-yl, etc.), in which manganese salt has the role of a chlorine atom-transfer catalyst as well as a redox mediator was developed. This method generates analogs of chlorosulfonylated products ArCH(Cl)CH2S(O)2R/ R1C(Cl)=CHS(O)2R of high regio- and stereoselectivity, which are derivatives of pharmaceutical drugs and natural products.

Category: chlorides-buliding-blocks, 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