CC1=CC=C(C=C1)S(=O)(=O)N(CC(=O)NC1=CC=C(C=C1)S(=O)(=O)N1CCCCC1)C1=CC(Cl)=C(Cl)C=C1

InChIKey=ZGIJCYFYXJIMJV-UHFFFAOYSA-N

C26H27Cl2N3O5S2

596.54

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Sulfanilides Alpha amino acids and derivatives Benzenesulfonamides Anilides Benzenesulfonyl compounds N-arylamides Dichlorobenzenes Piperidines Organosulfonamides Aryl chlorides Aminosulfonyl compounds Secondary carboxylic acid amides Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Alpha-amino acid or derivatives - Sulfanilide - Benzenesulfonamide - Anilide - Benzenesulfonyl group - N-arylamide - 1,2-dichlorobenzene - Halobenzene - Chlorobenzene - Piperidine - Organosulfonic acid amide - Aryl chloride - Aryl halide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organonitrogen compound - Organochloride - Organohalogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen 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