Compound Identification
SMILES
CC(=O)NC1=CC=C(C=C1)C(=O)CC(=O)C1=CC=CC=C1O
InChIKey
InChIKey=TZCUNIVJUUTVGM-UHFFFAOYSA-N
Formula
C17H15NO4
Mass
297.31
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
-
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
2'-Hydroxy-dihydrochalcones Cinnamylphenols Alkyl-phenylketones Butyrophenones Acetanilides N-acetylarylamines Benzoyl derivatives Aryl alkyl ketones 1-hydroxy-2-unsubstituted benzenoids Beta-diketones 1-hydroxy-4-unsubstituted benzenoids Acetamides Vinylogous acids Secondary carboxylic acid amides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
2'-hydroxy-dihydrochalcone - Retro-dihydrochalcone - Cinnamylphenol - Alkyl-phenylketone - Butyrophenone - Acetanilide - N-acetylarylamine - Anilide - Phenylketone - N-arylamide - Aryl ketone - Aryl alkyl ketone - Benzoyl - Phenol - 1-hydroxy-2-unsubstituted benzenoid - 1,3-diketone - 1-hydroxy-4-unsubstituted benzenoid - 1,3-dicarbonyl compound - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Acetamide - Carboxamide group - Ketone - Secondary carboxylic acid amide - Carboxylic acid derivative - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic homomonocyclic 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