Compound Identification
SMILES
CCB1OCC(O1)C1OC(OC2=CC=CC=C2)C2OB(CC)OC12
InChIKey
InChIKey=OZCFFIBVPPIMQI-UHFFFAOYSA-N
Formula
C16H22B2O6
Mass
331.97
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
Phenoxy compounds Phenol ethers Monosaccharides Tetrahydrofurans Dioxaborolanes Boronic acid esters Oxacyclic compounds Organic metalloid salts Acetals Monoalkylboranes Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenolic glycoside - Phenoxy compound - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Boronic acid ester - 1,3,2-dioxaborolane - Tetrahydrofuran - Boronic acid derivative - Oxacycle - Acetal - Organoheterocyclic compound - Organic metalloid salt - Monoalkylborane - Hydrocarbon derivative - Organoboron compound - Alkylborane - Organic salt - Aromatic heteropolycyclic 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