[O-][N+](=O)C1=CC=CC(=C1)C(=O)NC1=CC=CC(=C1)C(=O)C=CC1=CC=C(C=CC(=O)C2=CC(NC(=O)C3=CC(=CC=C3)[N+]([O-])=O)=CC=C2)C=C1

InChIKey=YFGZGTKFTXWVGS-UHFFFAOYSA-N

C38H26N4O8

666.646

Organic compounds

Phenylpropanoids and polyketides

Linear 1,3-diarylpropanoids

Chalcones and dihydrochalcones

Not available

Retrochalcones

Benzanilides Cinnamic acids and derivatives Benzamides Nitrobenzenes Aryl ketones Styrenes Benzoyl derivatives Nitroaromatic compounds Enones Acryloyl compounds Secondary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions

Aromatic homomonocyclic compounds

Retrochalcone - Benzanilide - Aromatic anilide - Cinnamic acid or derivatives - Benzamide - Benzoic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Benzoyl - Styrene - Aryl ketone - Benzenoid - Monocyclic benzene moiety - Alpha,beta-unsaturated ketone - Acryloyl-group - Enone - Organic nitro compound - Secondary carboxylic acid amide - Carboxamide group - C-nitro compound - Ketone - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Carboxylic acid derivative - Organic zwitterion - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic salt - 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