CCOC1=CC=C(\C=C\C(=O)C2=CC=C(NC(=O)C(\NC(=O)C3=CC=CC=C3)=C\C3=CC=CC=C3Cl)C=C2)C=C1

InChIKey=JBTUVSJXIDOZEV-MJBVXKRMSA-N

C33H27ClN2O4

551.04

Organic compounds

Phenylpropanoids and polyketides

Linear 1,3-diarylpropanoids

Chalcones and dihydrochalcones

Not available

Retrochalcones

Hippuric acids and derivatives N-acyl-alpha amino acids and derivatives Alpha amino acid amides Cinnamic acid amides Anilides Styrenes Aryl ketones Benzoyl derivatives Phenoxy compounds Phenol ethers N-arylamides Chlorobenzenes Alkyl aryl ethers Aryl chlorides Acryloyl compounds Enones Secondary carboxylic acid amides Hydrocarbon derivatives Organochlorides Organic oxides

Aromatic homomonocyclic compounds

Retrochalcone - Hippuric acid or derivatives - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Cinnamic acid amide - Cinnamic acid or derivatives - Alpha-amino acid or derivatives - Benzamide - Benzoic acid or derivatives - Anilide - Phenoxy compound - Benzoyl - Aryl ketone - Phenol ether - Styrene - N-arylamide - Halobenzene - Alkyl aryl ether - Chlorobenzene - Aryl chloride - Benzenoid - Aryl halide - Monocyclic benzene moiety - Acryloyl-group - Enone - Alpha,beta-unsaturated ketone - Secondary carboxylic acid amide - Ketone - Carboxamide group - Ether - Carboxylic acid derivative - Carbonyl group - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organohalogen compound - Organochloride - Hydrocarbon derivative - Aromatic homomonocyclic compound

This compound belongs to the class of organic compounds known as retrochalcones. These are a form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.

Not available