CAS 5462-25-9
:4-chloro-3-methylbenzenesulfonamide
Description:
4-Chloro-3-methylbenzenesulfonamide, with the CAS number 5462-25-9, is an organic compound that features a sulfonamide functional group attached to a chlorinated aromatic ring. This compound is characterized by its sulfonamide group (-SO2NH2), which contributes to its potential as a pharmaceutical intermediate or in agrochemical applications. The presence of the chloro group at the para position and a methyl group at the meta position on the benzene ring influences its reactivity and solubility properties. Typically, sulfonamides exhibit antibacterial activity, and the specific substitution pattern of this compound may affect its biological activity. It is generally a solid at room temperature and may be soluble in polar solvents. Safety data should be consulted for handling, as sulfonamides can pose health risks, including allergic reactions in sensitive individuals. Overall, 4-chloro-3-methylbenzenesulfonamide is of interest in various fields, including medicinal chemistry and materials science, due to its unique structural features.
Formula:C7H8ClNO2S
InChI:InChI=1/C7H8ClNO2S/c1-5-4-6(12(9,10)11)2-3-7(5)8/h2-4H,1H3,(H2,9,10,11)
SMILES:Cc1cc(ccc1Cl)S(=O)(=O)N
Synonyms:- 6-Chloro-m-toluenesulfonamide
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Found 1 products.
4-Chloro-3-methylbenzene-1-sulfonamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H8ClNO2SPurity:Min. 95%Molecular weight:205.66 g/mol
