Ingle, D. B.; Shingare, M. S. published the artcile< Synthesis of disulfonamides>, Electric Literature of 42413-03-6, the main research area is bactericide disulfonate preparation; sulfonamide bactericide preparation; thiazolesulfonamide benzenesulfonyl; thiophenesulfonamide benzenesulfonyl; coumarin thiophenesulfonamide benzenesulfonyl; acridine thiophenesulfonamide benzenesulfonyl; quinoline thiophenesulfonamide benzenesulfonyl.
RSO2NHSO2R1 (I; R = Ph, Cl-, Br-, Me-, NO2-, CO2H-, AcNH-substituted Ph; R1 = Ph, Cl-, Br-, NO2-, MeO-, AcNH-substituted Ph, 2-thienyl, dimethylthiazolyl, quinolyl, acetamidocoumarinyl) were prepared by amidation of R1SO2Cl with RSO2NH2. I were inactive against S. aureus, S. typhi and V. comma at 200 μg/mL.
Journal of the Indian Chemical Society published new progress about 42413-03-6. 42413-03-6 belongs to class chlorides-buliding-blocks, and the molecular formula is C7H6Cl2O2S, Electric Literature of 42413-03-6.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics