CN(NC(=O)C1=CSC(=N1)C1CCN(CC1)S(=O)(=O)C1=CC(Cl)=C(C)C=C1)C1=CC=CC=C1

InChIKey=JNHBAWMXUMDJPG-UHFFFAOYSA-N

C23H25ClN4O3S2

505.05

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides Benzenesulfonyl compounds Thiazolecarboxamides Phenylhydrazines 2,4-disubstituted thiazoles Chlorobenzenes Aryl chlorides Piperidines Organosulfonamides Heteroaromatic compounds Sulfonyls Carboxylic acid hydrazides Azacyclic compounds Hydrocarbon derivatives Organooxygen compounds Organic oxides Organochlorides Organonitrogen compounds

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Benzenesulfonyl group - Phenylhydrazine - Thiazolecarboxamide - Thiazolecarboxylic acid or derivatives - 2,4-disubstituted 1,3-thiazole - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Piperidine - Organosulfonic acid amide - Thiazole - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Sulfonyl - Azole - Carboxylic acid hydrazide - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organochloride - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur 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