Compound Identification
SMILES
CC1=CC=C(C=C1)C1OC(COCC2=CC=C(Cl)C=C2)C(OCC2=CC=C(Cl)C=C2)C1O
InChIKey
InChIKey=JCRFRNVHMVKZKM-UHFFFAOYSA-N
Formula
C26H26Cl2O4
Mass
473.39
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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Level 5
Glycosyl compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Glycosyl compounds
Direct Parent
Phenolic glycosides
Alternative Parents
C-glycosyl compounds Benzylethers Toluenes Chlorobenzenes Monosaccharides Aryl chlorides Tetrahydrofurans Secondary alcohols Oxacyclic compounds Dialkyl ethers Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenolic glycoside - C-glycosyl compound - Benzylether - Chlorobenzene - Halobenzene - Toluene - Monosaccharide - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Benzenoid - Tetrahydrofuran - Secondary alcohol - Ether - Dialkyl ether - Oxacycle - Organoheterocyclic compound - Organochloride - Organohalogen compound - Alcohol - Hydrocarbon derivative - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
External Descriptors
Not available