CC1=CC(C)=C(NS(=O)(=O)C2=C(NN=CC3=C(Cl)C=CC=C3Cl)C=CC(=C2)[N+]([O-])=O)C=C1

InChIKey=UGUJOVNNVVDNFB-UHFFFAOYSA-N

C21H18Cl2N4O4S

493.36

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes m-Xylenes Phenylhydrazines Nitroaromatic compounds Dichlorobenzenes 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

Aromatic homomonocyclic compounds

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