Cl.CC(C)(CC1CC2=CC=CC=C2C1)NC[C@@H](O)COC1=C(F)C(F)=CC(\C=C\C(O)=O)=C1

InChIKey=FJKLTTVFPDIDBY-UKKCZRDYSA-N

C25H30ClF2NO4

481.96

Organic compounds

Phenylpropanoids and polyketides

Cinnamic acids and derivatives

Hydroxycinnamic acids and derivatives

Not available

Coumaric acids and derivatives

Cinnamic acids Indanes Styrenes Phenoxy compounds Phenol ethers Alkyl aryl ethers Aralkylamines Fluorobenzenes Aryl fluorides Secondary alcohols 1,2-aminoalcohols Amino acids Monocarboxylic acids and derivatives Dialkylamines Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Hydrochlorides Organic oxides Organofluorides

Aromatic homopolycyclic compounds

Cinnamic acid - Coumaric acid or derivatives - Indane - Phenoxy compound - Phenol ether - Styrene - Aralkylamine - Alkyl aryl ether - Fluorobenzene - Halobenzene - Benzenoid - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Amino acid - Amino acid or derivatives - Secondary alcohol - 1,2-aminoalcohol - Secondary amine - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Ether - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Hydrochloride - Carbonyl group - Organonitrogen compound - Organooxygen compound - Alcohol - Organofluoride - Amine - Organic oxide - Organohalogen compound - Organic oxygen compound - Aromatic homopolycyclic compound

This compound belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Not available