Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C(C(C[N+]([O-])=O)C1=CC2=C(CCO2)C=C1)C(=O)C1=CC(F)=C(C=C1)C(C)=O

InChIKey

InChIKey=OVXLNUIKBVQCDE-UHFFFAOYSA-N

Formula

C23H22FNO7

Mass

443.427

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Subclass

Chalcones and dihydrochalcones

Intermediate Tree Nodes

Not available

Direct Parent

Retro-dihydrochalcones

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Retro-dihydrochalcone - Alkyl-phenylketone - Phenylbutylamine - Butyrophenone - Acetophenone - Coumaran - Phenylketone - Benzoyl - Aryl alkyl ketone - Aryl ketone - Beta-keto acid - Fatty acid ester - Fluorobenzene - Halobenzene - Alkyl aryl ether - Monocyclic benzene moiety - Fatty acyl - Aryl fluoride - Keto acid - Benzenoid - 1,3-dicarbonyl compound - Aryl halide - Vinylogous halide - Organic nitro compound - Carboxylic acid ester - Ketone - C-nitro compound - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organic oxoazanium - Organofluoride - Aldehyde - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic salt - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Organic zwitterion - Organohalogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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