COC1=CC=C(C=C1)N(CC(=O)NC1=C(OC)C=CC(Cl)=C1)S(=O)(=O)C1=C(C)ON=C1C

InChIKey=ZLJZMAJCNNXMFT-UHFFFAOYSA-N

C21H22ClN3O6S

479.93

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

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

Aromatic heteromonocyclic compounds

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