CC1=CC=C(C=C1)S(=O)(=O)N1CN2CN(CC(C2)(C1)C(=O)C1=CC=C(C=C1)[N+]([O-])=O)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey=GAAINDDUVSEEHA-UHFFFAOYSA-N

C27H28N4O7S2

584.66

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Alkyl-phenylketones Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes Aryl alkyl ketones Benzoyl derivatives Nitroaromatic compounds Diazinanes Organosulfonamides Sulfonyls Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organic salts Hydrocarbon derivatives Amines Organic oxides Organic cations

Aromatic heteropolycyclic compounds

N,n-disubstituted p-toluenesulfonamide - Alkyl-phenylketone - Benzenesulfonamide - Phenylketone - Benzenesulfonyl group - Nitrobenzene - Nitroaromatic compound - Benzoyl - Aryl ketone - Aryl alkyl ketone - Organosulfonic acid amide - 1,3-diazinane - Organic sulfonic acid or derivatives - Sulfonyl - Organosulfonic acid or derivatives - Ketone - C-nitro compound - Organic nitro compound - Azacycle - Organoheterocyclic compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Organosulfur compound - Organic salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic cation - Aromatic heteropolycyclic 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