Structure Information
Structure

Compound Identification

SMILES

CN1C(N)=C(C(=O)COC(=O)C(=CC2=CC=C(Cl)C=C2)C2=CC=C(F)C=C2)C(=O)N(C)C1=O

InChIKey

InChIKey=JPLNWTJBSBVWQG-UHFFFAOYSA-N

Formula

C23H19ClFN3O5

Mass

471.87

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Stilbenes

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Stilbenes

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Stilbene - Cinnamic acid or derivatives - Cinnamic acid ester - Styrene - Aryl alkyl ketone - Aryl ketone - Aminopyrimidine - Chlorobenzene - Fatty acid ester - Fluorobenzene - Halobenzene - Pyrimidone - Alpha-acyloxy ketone - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Pyrimidine - Fatty acyl - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Vinylogous amide - Heteroaromatic compound - Urea - Amino acid or derivatives - Lactam - Ketone - Carboxylic acid ester - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Azacycle - Primary amine - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Organohalogen compound - Organic nitrogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

External Descriptors

Not available

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