CC1=CC=CC(=C1)C(=CC1=CC=C(C=C1)[N+]([O-])=O)C(=O)NC1=CC(C)=C(C=C1)S(F)(=O)=O

InChIKey=LESXNOJUTKAIEB-UHFFFAOYSA-N

C23H19FN2O5S

454.47

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Not available

Not available

Stilbenes

Cinnamic acid amides Phenylacetamides Anilides Benzenesulfonyl compounds Nitrobenzenes Styrenes N-arylamides Nitroaromatic compounds Toluenes Sulfonyls Sulfonyl fluorides Organosulfonic acids and derivatives Secondary carboxylic acid amides Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Organic salts Hydrocarbon derivatives Organic zwitterions Carbonyl compounds Organic oxides

Aromatic homomonocyclic compounds

Stilbene - Cinnamic acid amide - Cinnamic acid or derivatives - Phenylacetamide - Benzenesulfonyl group - Anilide - Nitrobenzene - N-arylamide - Nitroaromatic compound - Styrene - Toluene - Benzenoid - Monocyclic benzene moiety - Organic sulfonic acid or derivatives - Sulfonyl - Sulfonyl halide - Sulfonyl fluoride - Organosulfonic acid or derivatives - C-nitro compound - Organic nitro compound - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organic 1,3-dipolar compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic zwitterion - 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