Compound Identification
SMILES
FC(F)(F)C1=CC=C(C=C1)[C@@H](CC(=O)C1=CC=CC=C1)[C@H]1OC(=O)C=C1
InChIKey
InChIKey=NVDKRTXQLNBDIG-AEFFLSMTSA-N
Formula
C20H15F3O3
Mass
360.332
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
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Class
Linear 1,3-diarylpropanoids
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Subclass
Chalcones and dihydrochalcones
- Level 5 Retro-dihydrochalcones
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Subclass
Chalcones and dihydrochalcones
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Class
Linear 1,3-diarylpropanoids
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Linear 1,3-diarylpropanoids
Subclass
Chalcones and dihydrochalcones
Intermediate Tree Nodes
Not available
Direct Parent
Retro-dihydrochalcones
Alternative Parents
Terpene lactones Alkyl-phenylketones Butyrophenones Trifluoromethylbenzenes Aromatic monoterpenoids Monocyclic monoterpenoids Aryl alkyl ketones Benzoyl derivatives Butenolides Enoate esters Lactones Oxacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Organofluorides Alkyl fluorides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Retro-dihydrochalcone - Terpene lactone - Alkyl-phenylketone - Butyrophenone - P-cymene - Trifluoromethylbenzene - Aromatic monoterpenoid - Monocyclic monoterpenoid - Monoterpenoid - Phenylketone - Aryl alkyl ketone - Aryl ketone - Benzoyl - Monocyclic benzene moiety - Benzenoid - 2-furanone - Dihydrofuran - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Lactone - Ketone - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Carboxylic acid derivative - Alkyl fluoride - Carbonyl group - Organohalogen compound - Organofluoride - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as retro-dihydrochalcones. These are a form of normal dihydrochalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.
External Descriptors
Not available