Compound Identification
SMILES
Cl.CNC1CC(C)(C)OC2=C1C=C1C(CC(C)(C)OC1=C2)C1=CC=C(Cl)C=C1
InChIKey
InChIKey=UZRUYZCPHQHMBJ-UHFFFAOYSA-N
Formula
C23H29Cl2NO2
Mass
422.39
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
-
Class
Neoflavonoids
- Subclass Prenylated neoflavonoids
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Class
Neoflavonoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Neoflavonoids
Subclass
Prenylated neoflavonoids
Intermediate Tree Nodes
Not available
Direct Parent
Prenylated neoflavonoids
Alternative Parents
Pyranoneoflavonoids Neoflavans Pyranochromenes 2,2-dimethyl-1-benzopyrans Chlorobenzenes Aralkylamines Alkyl aryl ethers Aryl chlorides Oxacyclic compounds Dialkylamines Organochlorides Hydrochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Prenylated neoflavonoid - Pyranoneoflavonoid - Neoflavan - Pyranochromene - 2,2-dimethyl-1-benzopyran - Chromane - Benzopyran - 1-benzopyran - Aralkylamine - Alkyl aryl ether - Chlorobenzene - Halobenzene - Benzenoid - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Ether - Secondary aliphatic amine - Oxacycle - Organoheterocyclic compound - Secondary amine - Organochloride - Organohalogen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Amine - Hydrochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
External Descriptors
Not available