COC1=C(Cl)C=CC(=C1)S(=O)(=O)NC1=CC=C(C=C1)C1=CSC(N\C=C2/C=CC=CC2=O)=N1

InChIKey=HPOQLNLCSHUGAP-DTQAZKPQSA-N

C23H18ClN3O4S2

499.98

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Phenoxy compounds O-quinomethanes Methoxybenzenes Anisoles 2,4-disubstituted thiazoles Alkyl aryl ethers Chlorobenzenes Organosulfonamides 2-amino-1,3-thiazoles Aryl chlorides Vinylogous amides Heteroaromatic compounds Aminosulfonyl compounds Enamines Azacyclic compounds Hydrocarbon derivatives Organochlorides Organic oxides

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Anisole - Phenoxy compound - O-quinomethane - Phenol ether - Quinomethane - Methoxybenzene - 2,4-disubstituted 1,3-thiazole - Alkyl aryl ether - Chlorobenzene - Halobenzene - 1,3-thiazol-2-amine - Aryl chloride - Aryl halide - Organosulfonic acid amide - Aminosulfonyl compound - Vinylogous amide - Thiazole - Sulfonyl - Azole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Cyclic ketone - Ketone - Azacycle - Organoheterocyclic compound - Enamine - Ether - Organochloride - Organic nitrogen compound - Amine - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organohalogen compound - 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