COC1=C(C=C(Cl)C=C1)N(CC(=O)NC1=CC=C(C=C1)C1=NC2=C(S1)C=C(C)C=C2)S(C)(=O)=O

InChIKey=RSDKXZHLEYWWEB-UHFFFAOYSA-N

C24H22ClN3O4S2

516.03

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Anilides Benzothiazoles Methoxyanilines Phenoxy compounds Anisoles N-arylamides Methoxybenzenes Alkyl aryl ethers Chlorobenzenes Organosulfonamides Aryl chlorides Organic sulfonamides Aminosulfonyl compounds Thiazoles Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Carbonyl compounds Organochlorides Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Alpha-amino acid or derivatives - Sulfanilide - 1,3-benzothiazole - Methoxyaniline - Anilide - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - N-arylamide - Alkyl aryl ether - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Organic sulfonic acid amide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Azole - Organosulfonic acid or derivatives - Heteroaromatic compound - Sulfonyl - Thiazole - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organic oxide - Organooxygen compound - Carbonyl group - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organochloride - Organohalogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.

Not available