CC1=CC(C)=C(NS(=O)(=O)C2=C(NN=C3CCS(=O)(=O)C4=C3C=C(F)C=C4)C=CC(=C2)[N+]([O-])=O)C=C1

InChIKey=INJOIKWLTCGAPO-UHFFFAOYSA-N

C23H21FN4O6S2

532.56

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Thiochromanes Benzenesulfonamides 1-benzothiopyrans Benzenesulfonyl compounds Nitrobenzenes m-Xylenes Phenylhydrazines Nitroaromatic compounds Thiopyrans Organosulfonamides Aryl fluorides Sulfones Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Hydrazones Organofluorides Organic salts Organic zwitterions Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

Thiochromane - Sulfanilide - Benzenesulfonamide - Nitrobenzene - Benzenesulfonyl group - Benzothiopyran - 1-benzothiopyran - M-xylene - Xylene - Phenylhydrazine - Nitroaromatic compound - Aryl fluoride - Organosulfonic acid amide - Thiopyran - Aryl halide - Sulfone - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - C-nitro compound - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Hydrazone - Organic oxoazanium - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organofluoride - Organic oxygen compound - Organohalogen compound - Hydrocarbon derivative - Organosulfur compound - Organic nitrogen compound - Organic oxide - Organic salt - Organic zwitterion - Aromatic heteropolycyclic 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