COC1=CC(=CC(OC)=C1OC)C(=O)\C=C\C1=C(O)C=CC(=C1)[N+]([O-])=O

InChIKey=QFWWGMAZQDMPCF-GQCTYLIASA-N

C18H17NO7

359.334

Organic compounds

Phenylpropanoids and polyketides

Linear 1,3-diarylpropanoids

Chalcones and dihydrochalcones

Not available

Retrochalcones

Cinnamylphenols Hydroxycinnamic acids and derivatives Nitrophenols Nitrobenzenes Anisoles Aryl ketones Benzoyl derivatives Styrenes Methoxybenzenes Nitroaromatic compounds Phenoxy compounds Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Acryloyl compounds Enones Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organonitrogen compounds Organic oxides Organic salts Organic zwitterions

Aromatic homomonocyclic compounds

Retrochalcone - Cinnamylphenol - Cinnamic acid or derivatives - Hydroxycinnamic acid or derivatives - Nitrophenol - Nitrobenzene - Anisole - Benzoyl - Phenoxy compound - Nitroaromatic compound - Phenol ether - Styrene - Aryl ketone - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Enone - Alpha,beta-unsaturated ketone - Acryloyl-group - Organic nitro compound - C-nitro compound - Ketone - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Ether - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organic salt - Organic zwitterion - Organic oxygen compound - 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