Structure Information
Structure

Compound Identification

SMILES

[O-]C(=O)C(F)(F)F.OC[C@H]1OC(OC2=CC=C(C=C2)[N+]#N)[C@H](O)[C@@H](O)[C@@H]1O

InChIKey

InChIKey=ABZYAAQXRVRCDZ-IMGORKQJSA-M

Formula

C14H15F3N2O8

Mass

396.275

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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

Not available

Substituents

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Phenoxy compound - Phenol ether - Monosaccharide - Monocyclic benzene moiety - Benzenoid - Oxane - Alpha-halocarboxylic acid - Alpha-halocarboxylic acid or derivatives - Organic diazonium salt - Secondary alcohol - Carboxylic acid salt - Carboxylic acid derivative - Carboxylic acid - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Oxacycle - Polyol - Acetal - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Primary alcohol - Organic zwitterion - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alkyl halide - Alkyl fluoride - Alcohol - 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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