Compound Identification
SMILES
ClC1=CC(Cl)=C(C=C1)C(=O)\C=C\C1=CC=C(OC2CCCCO2)C=C1
InChIKey
InChIKey=SJGMBZMJKHRFJM-IZZDOVSWSA-N
Formula
C20H18Cl2O3
Mass
377.26
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 Retrochalcones
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Subclass
Chalcones and dihydrochalcones
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Class
Linear 1,3-diarylpropanoids
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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
Retrochalcones
Alternative Parents
Cinnamic acids and derivatives Aryl ketones Styrenes Phenoxy compounds Phenol ethers Benzoyl derivatives Dichlorobenzenes Aryl chlorides Oxanes Enones Acryloyl compounds Vinylogous halides Oxacyclic compounds Acetals Organochlorides Aldehydes Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Retrochalcone - Cinnamic acid or derivatives - Benzoyl - Phenoxy compound - 1,3-dichlorobenzene - Phenol ether - Styrene - Aryl ketone - Chlorobenzene - Halobenzene - Aryl halide - Benzenoid - Monocyclic benzene moiety - Aryl chloride - Oxane - Vinylogous halide - Alpha,beta-unsaturated ketone - Acryloyl-group - Enone - Ketone - Organoheterocyclic compound - Oxacycle - Acetal - Aldehyde - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organohalogen compound - Organochloride - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as retrochalcones. These are a form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.
External Descriptors
Not available