CC1=CC=C(C=C1)S(=O)(=O)N1CCN(C(COCC2=CC(Cl)=C(Cl)C=C2)CC2=CC=CC=C2)C(=O)CC1

InChIKey=DTUQKRJJXMOUJJ-UHFFFAOYSA-N

C28H30Cl2N2O4S

561.52

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Amphetamines and derivatives Benzenesulfonamides Benzenesulfonyl compounds Benzylethers Dichlorobenzenes 1,4-diazepanes Organosulfonamides Aryl chlorides Sulfonyls Tertiary carboxylic acid amides Lactams Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organonitrogen compounds Organochlorides

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Amphetamine or derivatives - Benzenesulfonamide - Benzenesulfonyl group - Benzylether - 1,2-dichlorobenzene - 1,4-diazepane - Halobenzene - Diazepane - Chlorobenzene - Aryl chloride - Aryl halide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary carboxylic acid amide - Carboxamide group - Lactam - Ether - Dialkyl ether - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen 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