COC1=C(OC)C=C(C(=C1)C(F)(F)F)S(=O)(=O)NC1=CC(O[C@@H]2CCN(C)C2)=C(Cl)C=C1

InChIKey=BCKWOWPJUJPWNP-CYBMUJFWSA-N

C20H22ClF3N2O5S

494.91

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Trifluoromethylbenzenes Benzenesulfonamides Dimethoxybenzenes Benzenesulfonyl compounds Phenoxy compounds Anisoles Alkyl aryl ethers Chlorobenzenes Organosulfonamides Aryl chlorides N-alkylpyrrolidines Aminosulfonyl compounds Trialkylamines Azacyclic compounds Organochlorides Organofluorides Alkyl fluorides Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Dimethoxybenzene - O-dimethoxybenzene - Trifluoromethylbenzene - Benzenesulfonyl group - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - N-alkylpyrrolidine - Aryl chloride - Aryl halide - Organosulfonic acid amide - Aminosulfonyl compound - Pyrrolidine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Ether - Organic oxide - Organochloride - Organohalogen compound - Organic oxygen compound - Organofluoride - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alkyl fluoride - Alkyl halide - Amine - 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