Babu, Gogu V. Surendra team published research on ChemistrySelect in 2021 | 2905-24-0

Formula: C6H4BrClO2S, 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.

Organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. 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 names and applications. Formula: C6H4BrClO2S.

Babu, Gogu V. Surendra;Bhaskaran, Aathira;Sridhar, Balasubramanian;Rao, Tumula Venkateshwar;Parvathaneni, Sai Prathima research published 《 Ullmann Coupling Reaction of Bicyclic Amidines DBU/DBN with Aryl Halides: A Pathway to the Synthesis of ε-Caprolactam Derivatives》, the research content is summarized as follows. This paper demonstrated a selective, mild approach to copper iodide catalyzed Ullmann amination of aryl halides to synthesize N-alkylated derivatives of ε-caprolactam I [R = Ph, 4-ClC6H4, 3-pyridyl, etc; n = 1, 3]. The synthetic route involved an in-situ ring-opening of 1,8-diazabicyclo[5.4.0]undec-8-ene (DBU) followed by concurrent arylation with aryl halides in the presence of copper iodide as a catalyst under ligand-free conditions. This method provided wide variety of ε-caprolactam derivatives I in good to excellent yields in a single synthetic sequence. Similarly, other bicyclic amidines such as 1,5-diazabicyclo-[4.3.0]non-5-ene (DBN), and 1,5,7-triazabicyclo[4.4.0]-dec-5-ene (TBD) also showed good to very high reactivity.

Formula: C6H4BrClO2S, 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