CC1=CC=C(\C=C2/N=C(OC2=O)C2=CC=CC=C2N(CC=C)S(=O)(=O)C2=CC=C(C)C=C2)C=C1

InChIKey=FUSMYLUFKRCRHI-MOHJPFBDSA-N

C27H24N2O4S

472.56

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Sulfanilides Alpha amino acids and derivatives Benzenesulfonamides Benzenesulfonyl compounds 4-Hydrocarbylideneazlactones Organosulfonamides Aminosulfonyl compounds Monocarboxylic acids and derivatives Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds Organonitrogen compounds

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - 4-hydrocarbylideneazlactone - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Oxazoline - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as n,n-disubstituted p-toluenesulfonamides. These are p-toluenesulfonamide derivatives in which the sulfonamide moiety is N,N-disubstituted.

Not available