CC(=O)Nc1ccc(cc1)S(=O)(=O)Nc1cc(c(SC2=C(O)OC(C)(CCc3ccc(O)cc3)CC2=O)cc1C)C(C)(C)C

InChIKey=ZVAYUHKZJZHKSM-UHFFFAOYSA-N

C33H38N2O7S2

638.79

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Acetanilides Benzenesulfonamides Phenylpropanes N-acetylarylamines Benzenesulfonyl compounds Aryl thioethers Toluenes 1-hydroxy-2-unsubstituted benzenoids Dihydropyranones Organosulfonamides Vinylogous esters Vinylogous acids Acetamides Aminosulfonyl compounds Thioenol ethers Secondary carboxylic acid amides Cyclic ketones Oxacyclic compounds Sulfenyl compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Acetanilide - Sulfanilide - Benzenesulfonamide - N-acetylarylamine - Phenylpropane - Benzenesulfonyl group - Anilide - Aryl thioether - N-arylamide - 1-hydroxy-2-unsubstituted benzenoid - Toluene - Dihydropyranone - Phenol - Organosulfonic acid amide - Vinylogous ester - Vinylogous acid - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Sulfonyl - Organosulfonic acid or derivatives - Acetamide - Cyclic ketone - Carboxamide group - Secondary carboxylic acid amide - Thioenolether - Ketone - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Sulfenyl compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Organosulfur compound - Organic oxygen compound - Carbonyl group - 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