OCC1=CC=C(C=C1)[C@@H]1C[C@H](CN2CCC(CC2)N2C(=O)NC3=CC=CC=C23)O[C@@H](O1)C1=CC=C(NS(=O)(=O)C2=CC=CC=C2)C=C1

InChIKey=RUOOHYNELWDQLF-DCCHFUKUSA-N

C36H38N4O6S

654.78

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Benzimidazoles Benzyl alcohols Aralkylamines 1,3-dioxanes Piperidines Organosulfonamides N-substituted imidazoles Aminosulfonyl compounds Heteroaromatic compounds Trialkylamines Ureas Oxacyclic compounds Azacyclic compounds Acetals Organic oxides Organopnictogen compounds Primary alcohols Aromatic alcohols Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Benzenesulfonamide - Sulfanilide - Benzimidazole - Benzenesulfonyl group - Benzyl alcohol - Aralkylamine - Meta-dioxane - N-substituted imidazole - Piperidine - Organosulfonic acid amide - Azole - Imidazole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Urea - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Oxacycle - Acetal - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Alcohol - Primary alcohol - Amine - Aromatic alcohol - 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