Cl.OC1=CC=C(C=C1)[C@H]1SC2=C(O[C@H]1C1=CC=C(OCCN3CCCC3)C=C1)C(F)=C(O)C(F)=C2

InChIKey=VRVPXSOCJNUOGM-ZFGDHOEWSA-N

C26H26ClF2NO4S

522.0

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Not available

Not available

Stilbenes

Phenoxy compounds Phenol ethers O-fluorophenols 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Alkylarylthioethers Oxathiins Aryl fluorides Benzoxathiins N-alkylpyrrolidines Trialkylamines Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Hydrochlorides Organofluorides

Aromatic heteropolycyclic compounds

Stilbene - Phenoxy compound - Aryl thioether - Phenol ether - 2-halophenol - 2-fluorophenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkylarylthioether - 1,4-benzooxathiin - Benzenoid - N-alkylpyrrolidine - 1,4-oxathiin - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Pyrrolidine - Tertiary amine - Tertiary aliphatic amine - Thioether - Oxacycle - Azacycle - Ether - Organoheterocyclic compound - Organic nitrogen compound - Organohalogen compound - Hydrochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Not available