[O-][N+](=O)C1=CC(=CNC2=CC(Cl)=C(Cl)C=C2NS(=O)(=O)C2=CC=CC=C2)C(=O)C=C1

InChIKey=HSUJUPUBEFOXPQ-UHFFFAOYSA-N

C19H13Cl2N3O5S

466.29

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Aniline and substituted anilines O-quinomethanes Dichlorobenzenes Organosulfonamides Aryl chlorides Vinylogous amides Aminosulfonyl compounds C-nitro compounds Propargyl-type 1,3-dipolar organic compounds Allylamines Organic oxoazanium compounds Enamines Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Organochlorides

Aromatic homomonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - 1,2-dichlorobenzene - Aniline or substituted anilines - O-quinomethane - Quinomethane - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Vinylogous amide - Aminosulfonyl compound - Sulfonyl - Organic nitro compound - Ketone - C-nitro compound - Cyclic ketone - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Allylamine - Enamine - Organic oxoazanium - Organic oxygen compound - Organohalogen compound - Organic salt - Organic nitrogen compound - Amine - Organochloride - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organic oxide - 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