Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC=CC(=C1)N1C(=O)C2C(C1=O)C1(C(=O)C2(C(=C1C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=C(Cl)C=C1)C1=CC=C(Cl)C=C1

InChIKey

InChIKey=ALQYNJMXOUJUNP-UHFFFAOYSA-N

Formula

C39H24Cl2N2O5

Mass

671.53

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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 - 1-phenylpyrrolidine - Isoindolone - Nitrobenzene - Isoindole or derivatives - Isoindoline - Nitroaromatic compound - Chlorobenzene - Halobenzene - Aryl chloride - Benzenoid - Monocyclic benzene moiety - 2-pyrrolidone - Pyrrolidone - Aryl halide - Carboxylic acid imide, n-substituted - Carboxylic acid imide - Pyrrolidine - Pyrrole - Dicarboximide - Organic nitro compound - Ketone - Lactam - C-nitro compound - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Carbonyl group - Organic oxide - Organic salt - Organic oxygen compound - Organic nitrogen compound - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Organochloride - Hydrocarbon derivative - Organohalogen compound - 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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