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. Synthetic Route of 2905-24-0.
Chen, Dan;Lin, Li;Peng, Xiaoyan;Yu, Xinyi;Yang, Zhonglie;Liu, Yutong;Zhang, Xiaobin;Li, Jiahong;Jiang, Hezhong research published 《 Transition-metal-free NaI-mediated reaction of aryl sulfonyl chloride with alkynes: Synthesis of (E)-β-iodovinyl sulfones》, the research content is summarized as follows. A novel protocol for synthesis of (E)-β-iodovinyl sulfones via NaI-mediated aryl sulfonyl chloride with alkynes were described, featuring transition-metal-free condition, com. available substrates, convenient operation, as well as good functional group compatibility. A wide variety of substrate application and good functional group tolerance were provided by this approach, giving multiple (E)-β-iodovinyl sulfones analogs with excellent yields (up to 98%, >4 g scale).
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., Synthetic Route of 2905-24-0
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics