COC1=CC(=CC(OC)=C1OC)C(=O)C(=CC1=CC(=C(OC)C=C1)[N+]([O-])=O)C1=CC=C(C)C=C1

InChIKey=SJYADFMBLHITPY-UHFFFAOYSA-N

C26H25NO7

463.486

Organic compounds

Phenylpropanoids and polyketides

Linear 1,3-diarylpropanoids

Chalcones and dihydrochalcones

Not available

Retrochalcones

Stilbenes Cinnamic acids and derivatives Nitrophenyl ethers Methoxyanilines Anisoles Aryl ketones Benzoyl derivatives Styrenes Methoxybenzenes Nitroaromatic compounds Phenoxy compounds Alkyl aryl ethers Toluenes Alpha-branched alpha,beta-unsaturated ketones Acryloyl compounds Enones Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organic oxides Organic salts Organonitrogen compounds Organic cations

Aromatic homomonocyclic compounds

Retrochalcone - Stilbene - Cinnamic acid or derivatives - Nitrophenyl ether - Nitrobenzene - Methoxyaniline - Styrene - Phenoxy compound - Phenol ether - Nitroaromatic compound - Aryl ketone - Anisole - Methoxybenzene - Benzoyl - Alkyl aryl ether - Toluene - Benzenoid - Alpha-branched alpha,beta-unsaturated-ketone - Monocyclic benzene moiety - Alpha,beta-unsaturated ketone - Acryloyl-group - Enone - Organic nitro compound - Ketone - C-nitro compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Ether - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic cation - 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