Structure Information
Structure

Compound Identification

SMILES

OCC1O[C@@H](OC2=C(Cl)C=C(C=C2)C(=C2\C=CC(=O)C(Cl)=C2)\C2=CC=CC=C2S(O)(=O)=O)C(O)[C@H](O)[C@H]1O

InChIKey

InChIKey=YOUWVNCQJOMMEU-MNEBIYGUSA-N

Formula

C25H22Cl2O10S

Mass

585.4

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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

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Diphenylmethane - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Benzenesulfonate - Benzenesulfonyl group - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - P-quinomethane - Phenoxy compound - Phenol ether - Quinomethane - Halobenzene - Chlorobenzene - Monocyclic benzene moiety - Fatty acyl - Aryl halide - Monosaccharide - Aryl chloride - Oxane - Benzenoid - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Alpha-haloketone - Alpha-chloroketone - Cyclic ketone - Secondary alcohol - Ketone - Polyol - Oxacycle - Chloroalkene - Haloalkene - Vinyl chloride - Vinyl halide - Acetal - Organoheterocyclic compound - Organochloride - Carbonyl group - Alcohol - Primary alcohol - Aldehyde - Hydrocarbon derivative - Organic oxide - Organosulfur compound - 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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