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

InChIKey=JAARYQYYOHWEJC-UHFFFAOYSA-N

C44H41N7O20S6

1180.2

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Nitrobenzenes Benzenesulfonyl compounds Nitroaromatic compounds Organosulfonic acids and derivatives Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organonitrogen compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations

Aromatic homomonocyclic compounds

Benzenesulfonamide - Sulfanilide - Nitrobenzene - Benzenesulfonyl group - Nitroaromatic compound - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - C-nitro compound - Organic nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic oxygen compound - Organic salt - Organosulfur compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic homomonocyclic 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