COC1=CC=CC=C1NS(=O)(=O)C1=CC(=C(N\N=C/C=C/C2=CC=CC=C2[N+]([O-])=O)C=C1)[N+]([O-])=O

InChIKey=YLDWEHIXIVHXFW-HWTQHHHFSA-N

C22H19N5O7S

497.48

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Methoxyanilines Nitrobenzenes Styrenes Phenylhydrazines Phenoxy compounds Anisoles Methoxybenzenes Nitroaromatic compounds Alkyl aryl ethers Organosulfonamides Aminosulfonyl compounds Organic oxoazanium compounds Hydrazones Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives Organic salts Organic zwitterions Organic oxides

Aromatic homomonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Nitrobenzene - Methoxyaniline - Phenoxy compound - Nitroaromatic compound - Anisole - Phenol ether - Methoxybenzene - Phenylhydrazine - Styrene - Alkyl aryl ether - Organosulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - C-nitro compound - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Ether - Hydrazone - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organic salt - Organic oxygen compound - 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