COC1=C(OC)C=C(C=NNC2=C(C=C(C=C2)S(=O)(=O)NC2=CC=C(Cl)C=C2)[N+]([O-])=O)C=C1

InChIKey=HJLMAFIAHCNQMI-UHFFFAOYSA-N

C21H19ClN4O6S

490.92

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Dimethoxybenzenes Benzenesulfonyl compounds Nitrobenzenes Anisoles Phenylhydrazines Phenoxy compounds Nitroaromatic compounds Alkyl aryl ethers Chlorobenzenes Organosulfonamides Aryl chlorides Aminosulfonyl compounds Hydrazones Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic oxides Hydrocarbon derivatives Organic salts Organic zwitterions Organochlorides

Aromatic homomonocyclic compounds

Sulfanilide - Dimethoxybenzene - O-dimethoxybenzene - Benzenesulfonamide - Nitrobenzene - Benzenesulfonyl group - Phenylhydrazine - Phenol ether - Phenoxy compound - Nitroaromatic compound - Anisole - Methoxybenzene - Chlorobenzene - Alkyl aryl ether - Halobenzene - Organosulfonic acid amide - Aryl chloride - Aryl halide - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Organic nitro compound - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Ether - Organic 1,3-dipolar compound - Hydrazone - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organic zwitterion - Organic salt - Organohalogen compound - Organic oxide - Organochloride - Organonitrogen compound - Organooxygen 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