CC1=CC=C(C=C1)S(=O)(=O)NC1=C(C=C(C=C1)N=CC1=CC=C(C=C1)[N+]([O-])=O)C1=NC2=CC=CC=C2S1

InChIKey=JLEVITHTBJBAEJ-UHFFFAOYSA-N

C27H20N4O4S2

528.6

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds

P-toluenesulfonamides

Benzenesulfonamides Sulfanilides Benzenesulfonyl compounds Benzothiazoles Nitrobenzenes Nitroaromatic compounds Organosulfonamides Aminosulfonyl compounds Heteroaromatic compounds Thiazoles Shiff bases Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxides Organic zwitterions Hydrocarbon derivatives Organic salts

Aromatic heteropolycyclic compounds

P-toluenesulfonamide - Benzenesulfonamide - Sulfanilide - 1,3-benzothiazole - Benzenesulfonyl group - Nitrobenzene - Nitroaromatic compound - Organosulfonic acid amide - Azole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiazole - Aminosulfonyl compound - C-nitro compound - Shiff base - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Aldimine - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Organonitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organosulfur compound - Organic oxide - Organic nitrogen compound - Imine - Organic salt - Organic zwitterion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as p-toluenesulfonamides. These are aromatic heterocyclic compounds containing a toluene that is p-substituted with a sulfonamide group.

Not available