OCC1=CC=C(C=C1)[C@@H]1C[C@H](CN2CCN(CC3=CC=CC=C3)CC2)O[C@@H](O1)C1=CC=C(NS(=O)(=O)C2=CC=CC=C2)C=C1

InChIKey=RIHXACJPXBQEEK-SMXONETASA-N

C35H39N3O5S

613.77

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Phenylmethylamines Benzylamines Benzyl alcohols N-alkylpiperazines Aralkylamines 1,3-dioxanes Organosulfonamides Aminosulfonyl compounds Trialkylamines Oxacyclic compounds Acetals Azacyclic compounds Aromatic alcohols Hydrocarbon derivatives Organic oxides Organopnictogen compounds Primary alcohols

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Benzyl alcohol - Benzylamine - Phenylmethylamine - Aralkylamine - N-alkylpiperazine - Meta-dioxane - 1,4-diazinane - Piperazine - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Tertiary aliphatic amine - Tertiary amine - Acetal - Organoheterocyclic compound - Oxacycle - Azacycle - Aromatic alcohol - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Organic nitrogen compound - Alcohol - 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