COC1=CC=CC=C1NS(=O)(=O)C1=C(NN=CC2=C(Cl)C=C(Cl)C=C2)C=CC(=C1)[N+]([O-])=O

InChIKey=MSWYLDHUWLAZPH-UHFFFAOYSA-N

C20H16Cl2N4O5S

495.33

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

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

Aromatic homomonocyclic compounds

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