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

InChIKey=QASYGLKIOGTULW-XODNFHPESA-N

C23H20F4N4O7S

572.49

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

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

Aromatic homomonocyclic compounds

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