CC1=C(NC(=O)CSC2=NN=C(O2)C2=CC=NC=C2)C=C(C=C1)S(=O)(=O)N1CCCCC1

InChIKey=GCZNCVZIXLPKAX-UHFFFAOYSA-N

C21H23N5O4S2

473.57

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides Anilides Benzenesulfonyl compounds N-arylamides Alkylarylthioethers Piperidines Organosulfonamides Pyridines and derivatives 1,3,4-oxadiazoles Heteroaromatic compounds Sulfonyls Secondary carboxylic acid amides Oxacyclic compounds Sulfenyl compounds Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Anilide - Benzenesulfonyl group - N-arylamide - Aryl thioether - Alkylarylthioether - Organosulfonic acid amide - Pyridine - Piperidine - Sulfonyl - Azole - 1,3,4-oxadiazole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Heteroaromatic compound - Oxadiazole - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - 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