Structure Information
Structure

Compound Identification

SMILES

OCC1OC(OC2=CC=C(Cl)C=C2)C(O)C1O

InChIKey

InChIKey=IQZCEOJXPCSWOV-UHFFFAOYSA-N

Formula

C11H13ClO5

Mass

260.67

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Taxonomic Classification

Taxonomy Tree

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

O-glycosyl compounds Pentoses Phenoxy compounds Phenol ethers Chlorobenzenes Aryl chlorides Oxolanes Secondary alcohols Oxacyclic compounds Acetals Primary alcohols Organochlorides Hydrocarbon derivatives

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenolic glycoside - O-glycosyl compound - Pentose monosaccharide - Phenoxy compound - Phenol ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Oxolane - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Organochloride - Primary alcohol - Hydrocarbon derivative - Alcohol - Organohalogen compound - 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

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