Structure Information
Structure

Compound Identification

SMILES

COC1=CC=CC(=C1)C(=CC1=CC=C(C=C1)[N+]([O-])=O)C(=O)NC1=CC=C(C=C1)S(F)(=O)=O

InChIKey

InChIKey=XAYKQRHICAGEEY-UHFFFAOYSA-N

Formula

C22H17FN2O6S

Mass

456.44

Export to:

JSON SDF CSV

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 or derivatives - Cinnamic acid amide - Phenylacetamide - Nitrobenzene - Anilide - Benzenesulfonyl group - Nitroaromatic compound - Methoxybenzene - Phenol ether - Phenoxy compound - Styrene - N-arylamide - Anisole - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Sulfonyl fluoride - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Sulfonyl - Sulfonyl halide - Carboxamide group - Organic nitro compound - C-nitro compound - Secondary carboxylic acid amide - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organic oxoazanium - Ether - Organic zwitterion - Organic salt - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organosulfur compound - 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

Previous Back Next