[Br-].CC(=O)OC\C(=C(/C(=O)OCC[N+](C)(C)C)C1=CC(F)=C(F)C=C1)C1=CC=C(C=C1)S(C)(=O)=O

InChIKey=WUWCKMMTTHIGTD-NMSJBYGBSA-M

C24H28BrF2NO6S

576.45

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Not available

Not available

Stilbenes

Cinnamic acid esters Acyl cholines Benzenesulfonyl compounds Fluorobenzenes Fatty acid esters Aryl fluorides Dicarboxylic acids and derivatives Tetraalkylammonium salts Sulfones Enoate esters Hydrocarbon derivatives Organic bromide salts Carbonyl compounds Organic oxides Organofluorides Amines Organopnictogen compounds

Aromatic homomonocyclic compounds

Stilbene - Cinnamic acid ester - Cinnamic acid or derivatives - Acyl choline - Benzenesulfonyl group - Halobenzene - Fluorobenzene - Fatty acid ester - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - Fatty acyl - Sulfonyl - Sulfone - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Quaternary ammonium salt - Tetraalkylammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic salt - Organic bromide salt - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic 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