COCCNC1=C(C=C(S1)S(=O)(=O)NC1=CC=C(Cl)C=C1)[N+]([O-])=O

InChIKey=IBDGLYLVYNQYGT-UHFFFAOYSA-N

C13H14ClN3O5S2

391.84

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

3-nitrothiophenes 2,3,5-trisubstituted thiophenes Nitroaromatic compounds Chlorobenzenes Organosulfonamides 2-aminothiophenes Aryl chlorides Aminosulfonyl compounds Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Amines Organic salts Organic zwitterions Organochlorides

Aromatic heteromonocyclic compounds

Sulfanilide - 3-nitrothiophene - Nitrothiophene - 2,3,5-trisubstituted thiophene - Nitroaromatic compound - Chlorobenzene - Halobenzene - Aryl chloride - Organosulfonic acid amide - Aryl halide - 2-aminothiophene - Thiophene - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Dialkyl ether - Ether - Organoheterocyclic compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organochloride - Organic oxygen compound - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Organic salt - Organic oxide - Amine - Organic zwitterion - Aromatic heteromonocyclic 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