Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC=C(C=C(C(=O)NC2=CC=C(C=C2)S(F)(=O)=O)C2=CC(Cl)=CC=C2)C=C1

InChIKey

InChIKey=FHVVKFMPGCMIQV-UHFFFAOYSA-N

Formula

C21H14ClFN2O5S

Mass

460.86

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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 homomonocyclic compounds

Substituents

Stilbene - Cinnamic acid amide - Cinnamic acid or derivatives - Phenylacetamide - Nitrobenzene - Benzenesulfonyl group - Anilide - Nitroaromatic compound - Styrene - N-arylamide - Chlorobenzene - Halobenzene - Benzenoid - Aryl chloride - Monocyclic benzene moiety - Aryl halide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl fluoride - Sulfonyl halide - Sulfonyl - Organic nitro compound - Secondary carboxylic acid amide - C-nitro compound - Carboxamide group - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organic zwitterion - Organic oxide - Organohalogen compound - Organochloride - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Hydrocarbon derivative - Organic salt - Aromatic homomonocyclic 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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