ClC1=CC=CC(Cl)=C1\C=C\C(=O)C1=CC=C(NC(=O)C(\NC(=O)C2=CC=CC=C2)=C\C2=CC=CC3=CC=CC=C23)C=C1

InChIKey=WXHXIWTZFLSVHR-YOXDIMGBSA-N

C35H24Cl2N2O3

591.49

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 Naphthalenes Anilides N-arylamides Dichlorobenzenes Benzoyl derivatives Aryl ketones Styrenes Aryl chlorides Enones Acryloyl compounds Secondary carboxylic acid amides Organic oxides Hydrocarbon derivatives Organochlorides

Aromatic homopolycyclic 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 - Naphthalene - Benzamide - Benzoic acid or derivatives - Anilide - Benzoyl - Aryl ketone - 1,3-dichlorobenzene - N-arylamide - Styrene - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Enone - Acryloyl-group - Alpha,beta-unsaturated ketone - Secondary carboxylic acid amide - Ketone - Carboxamide group - Carboxylic acid derivative - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organohalogen compound - Organochloride - Organonitrogen compound - Organic nitrogen compound - Aromatic homopolycyclic 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