Compound Identification
SMILES
COC(=O)C(=C(\Br)C1=CC=C(C=C1)[N+]([O-])=O)\C1=CC=CC=C1
InChIKey
InChIKey=HTRKCVDAWCULDN-CCEZHUSRSA-N
Formula
C16H12BrNO4
Mass
362.179
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Stilbenes
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Stilbenes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Stilbenes
Alternative Parents
Cinnamic acid esters Nitrobenzenes Nitroaromatic compounds Fatty acid esters Methyl esters Enoate esters Vinylogous halides Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Vinyl bromides Monocarboxylic acids and derivatives Bromoalkenes Organobromides Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organonitrogen compounds Organic cations
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Stilbene - Cinnamic acid or derivatives - Cinnamic acid ester - Nitrobenzene - Nitroaromatic compound - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Vinylogous halide - Methyl ester - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Organic nitro compound - Carboxylic acid ester - C-nitro compound - Carboxylic acid derivative - Bromoalkene - Haloalkene - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic 1,3-dipolar compound - Vinyl bromide - Vinyl halide - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organic salt - Organic oxygen compound - 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