Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](CCl)O[C@@H](OC2=CC=C(C=C2)N=[N+]=[N-])[C@@H](O)[C@H]1O

InChIKey

InChIKey=WWMGAQUXQNEPDE-LDMBFOFVSA-N

Formula

C12H14ClN3O5

Mass

315.71

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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 - O-glycosyl compound - Phenoxy compound - Phenol ether - Phenylazide - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Secondary alcohol - Azo compound - Azo imide - Oxacycle - Polyol - Organoheterocyclic compound - Acetal - Organic zwitterion - Organochloride - Organohalogen compound - Organic nitrogen compound - Alcohol - Organonitrogen compound - Alkyl chloride - Organopnictogen compound - Alkyl halide - Organic salt - 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

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