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

InChIKey=CMJOWVSLIJXUQR-UHFFFAOYSA-N

C22H16BrF3N4O5S

585.35

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Trifluoromethylbenzenes Alpha amino acids and derivatives Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes Nitroaromatic compounds Bromobenzenes Organosulfonamides Aryl bromides Aminosulfonyl compounds Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Organobromides Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides Organofluorides Organonitrogen compounds

Aromatic homomonocyclic compounds

Alpha-amino acid or derivatives - Sulfanilide - Trifluoromethylbenzene - Benzenesulfonamide - Nitrobenzene - Benzenesulfonyl group - Nitroaromatic compound - Halobenzene - Bromobenzene - Organosulfonic acid amide - Aryl bromide - Aryl halide - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Organic sulfonic acid or derivatives - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organobromide - Organic oxygen compound - Organohalogen compound - Organic nitrogen compound - Alkyl halide - Alkyl fluoride - Carbonyl group - Organic salt - Hydrocarbon derivative - Organic oxide - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic zwitterion - 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