[O-][N+](=O)C1=CC=CC(\C=C\S(=O)(=O)NC2=CC(OCC3=CN(CC4=CC5=CC=CC=C5N4)N=N3)=CC=C2)=C1

InChIKey=OIDAKDQOMKBOIG-VAWYXSNFSA-N

C26H22N6O5S

530.56

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Indoles Nitrobenzenes Nitroaromatic compounds Phenol ethers Phenoxy compounds Styrenes Alkyl aryl ethers Organosulfonamides Organic sulfonamides Substituted pyrroles Triazoles Aminosulfonyl compounds Heteroaromatic compounds Organic oxoazanium compounds Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Organonitrogen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Sulfanilide - Indole or derivatives - Indole - Nitrobenzene - Phenoxy compound - Styrene - Phenol ether - Nitroaromatic compound - Alkyl aryl ether - Organosulfonic acid amide - Substituted pyrrole - Organic sulfonic acid amide - Pyrrole - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Heteroaromatic compound - 1,2,3-triazole - Azole - Organic nitro compound - C-nitro compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Organic oxoazanium - Azacycle - Allyl-type 1,3-dipolar organic compound - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic 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