COC1=CC=C(C=C1)N(CC(C)(Cl)CSCC(C)(Cl)CN(C1=CC=C(OC)C=C1)S(=O)(=O)C1=CC=C(C)C=C1)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey=YTMYBGNRVMYHQO-UHFFFAOYSA-N

C36H42Cl2N2O6S3

765.82

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides Sulfanilides Benzenesulfonyl compounds Methoxyanilines Anisoles Phenoxy compounds Methoxybenzenes Sulfur mustard compounds Alkyl aryl ethers Organosulfonamides Aminosulfonyl compounds Dialkylthioethers Sulfenyl compounds Organic oxides Alkyl chlorides Hydrocarbon derivatives Organochlorides Organonitrogen compounds

Aromatic homomonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Methoxyaniline - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Sulfur mustard - Organosulfonic acid amide - Sulfonyl - Aminosulfonyl compound - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Ether - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Alkyl chloride - Aromatic homomonocyclic 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