[O-][N+](=O)C1=C(NN=CC2=CC=CC=C2C(F)(F)F)C=CC(=C1)S(=O)(=O)NC1=CC(Cl)=CC=C1

InChIKey=HHCDMTLNHWUTCW-UHFFFAOYSA-N

C20H14ClF3N4O4S

498.86

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Trifluoromethylbenzenes Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes Phenylhydrazines Nitroaromatic compounds Chlorobenzenes Organosulfonamides Aryl chlorides Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Hydrazones Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Organochlorides Organofluorides Alkyl fluorides

Aromatic homomonocyclic compounds

Trifluoromethylbenzene - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Nitrobenzene - Nitroaromatic compound - Phenylhydrazine - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Organic nitro compound - C-nitro compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Hydrazone - Organic oxoazanium - Organic zwitterion - Organochloride - Organofluoride - Organohalogen compound - Organic salt - Alkyl halide - Organonitrogen compound - Alkyl fluoride - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organosulfur 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