CC1=CC=C(C=C1)S(=O)(=O)N1CCN(CC1)C1=CC=C(C=C1)[N+]([O-])=O

InChIKey=SYVCJFNSTBNTRR-UHFFFAOYSA-N

C17H19N3O4S

361.42

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Phenylpiperazines N-arylpiperazines Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes Aniline and substituted anilines Dialkylarylamines Nitroaromatic compounds Organosulfonamides Sulfonyls Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - N-arylpiperazine - Phenylpiperazine - Benzenesulfonamide - Nitrobenzene - Benzenesulfonyl group - Nitroaromatic compound - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - 1,4-diazinane - Organosulfonic acid amide - Piperazine - Organosulfonic acid or derivatives - Sulfonyl - Organic sulfonic acid or derivatives - Tertiary amine - C-nitro compound - Organic nitro compound - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organosulfur compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - 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