Structure Information
Structure

Compound Identification

SMILES

OCC1OC(OC2=CC=C(C=C2)[N+]([O-])=O)C(O)C(O)C1O

InChIKey

InChIKey=IFBHRQDFSNCLOZ-UHFFFAOYSA-N

Formula

C12H15NO8

Mass

301.251

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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 - Hexose monosaccharide - O-glycosyl compound - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - C-nitro compound - Organic nitro compound - Secondary alcohol - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Acetal - Oxacycle - Organic oxoazanium - Organoheterocyclic compound - Polyol - Organopnictogen compound - Organic oxide - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Organic zwitterion - 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

META CYC (CPD0-2062) : a small molecule

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