Compound Identification
SMILES
CN1C=C[N+](C)=C1C(O)(C(=NC1=CC=CC=C1)C1=CC=C(Cl)C=C1)C1=CC=C(Br)C=C1
InChIKey
InChIKey=OQWOKGIWFNYJDQ-UHFFFAOYSA-N
Formula
C25H22BrClN3O
Mass
495.82
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
Bromobenzenes Chlorobenzenes Aryl bromides Aryl chlorides N-substituted imidazoles Tertiary alcohols Secondary ketimines Azomethines Heteroaromatic compounds Azacyclic compounds Aromatic alcohols Hydrocarbon derivatives Organobromides Organochlorides Organopnictogen compounds Organic cations
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Stilbene - Halobenzene - Chlorobenzene - Bromobenzene - N-substituted imidazole - Aryl bromide - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Tertiary alcohol - Azole - Secondary ketimine - Imidazole - Azomethine - Heteroaromatic compound - Ketimine - Organoheterocyclic compound - Azacycle - Alcohol - Organic nitrogen compound - Organohalogen compound - Imine - Organobromide - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic cation - Aromatic heteromonocyclic 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