Compound Identification
SMILES
COC1=CC(O)=C(C(=O)C=CC2=CC=C(SC)C=C2)C(OC)=C1
InChIKey
InChIKey=UAHKGRIMCHVSAP-UHFFFAOYSA-N
Formula
C18H18O4S
Mass
330.4
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 2'-Hydroxychalcones
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Subclass
Chalcones and dihydrochalcones
-
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
2'-Hydroxychalcones
Alternative Parents
Cinnamylphenols Cinnamic acids and derivatives Dimethoxybenzenes Methoxyphenols Anisoles Aryl ketones Benzoyl derivatives Thiophenol ethers Styrenes Phenoxy compounds Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids Alkylarylthioethers 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Acryloyl compounds Enones Sulfenyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
2'-hydroxychalcone - Cinnamylphenol - Cinnamic acid or derivatives - Methoxyphenol - Dimethoxybenzene - M-dimethoxybenzene - Phenoxy compound - Phenol ether - Styrene - Benzoyl - Thiophenol ether - Aryl thioether - Aryl ketone - Methoxybenzene - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkylarylthioether - Alkyl aryl ether - Phenol - Benzenoid - Monocyclic benzene moiety - Enone - Alpha,beta-unsaturated ketone - Vinylogous acid - Acryloyl-group - Ketone - Ether - Thioether - Sulfenyl compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.
External Descriptors
Not available