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

InChIKey=RFTVRRQJUSNBAK-UHFFFAOYSA-N

C29H25N5O8S2

635.67

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Nitrotoluenes Nitrobenzenes Nitroaromatic compounds Organosulfonamides Pyrazolines Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organic oxides Organic zwitterions Organonitrogen compounds Organopnictogen compounds

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Nitrobenzene - Benzenesulfonyl group - Nitrotoluene - Nitroaromatic compound - Toluene - Organosulfonic acid amide - Pyrazoline - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - 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 - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organonitrogen compound - Organic zwitterion - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.

Not available