Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)OC(=O)CC(C(=O)C1=C(O)C=CC(Br)=C1)C1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=ROBWONIDVBQSLK-UHFFFAOYSA-N

Formula

C20H20BrNO6

Mass

450.285

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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 - Alkyl-phenylketone - Butyrophenone - Nitrobenzene - Phenylketone - Gamma-keto acid - 4-bromophenol - Nitroaromatic compound - 4-halophenol - Aryl ketone - Aryl alkyl ketone - Benzoyl - Halobenzene - Fatty acid ester - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Bromobenzene - Keto acid - Benzenoid - Fatty acyl - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Vinylogous acid - Ketone - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Organic oxoazanium - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Organic oxygen compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic salt - Hydrocarbon derivative - Organic oxide - Organic cation - 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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