Structure Information
Structure

Compound Identification

SMILES

[Cl-].COC1=CC=C(\C=C(\C(=O)OC2CC3CCC(C2)[NH+]3C)C2=CC=C(Cl)C=C2)C=C1

InChIKey

InChIKey=FCBOYQCSPOSEDZ-PUZWSPMBSA-N

Formula

C24H27Cl2NO3

Mass

448.38

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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 heteropolycyclic compounds

Substituents

Stilbene - Cinnamic acid ester - Cinnamic acid or derivatives - Tropane alkaloid - Phenoxy compound - Anisole - Styrene - Methoxybenzene - Phenol ether - Alkyl aryl ether - Chlorobenzene - Fatty acid ester - Halobenzene - Benzenoid - Piperidine - Fatty acyl - N-alkylpyrrolidine - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Pyrrolidine - Quaternary ammonium salt - Tertiary amine - Tertiary aliphatic amine - Amino acid or derivatives - Carboxylic acid ester - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Ether - Amine - Organic oxygen compound - Organic salt - Organic nitrogen compound - Organic chloride salt - Organohalogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic cation - Aromatic heteropolycyclic 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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