Structure Information
Structure

Compound Identification

SMILES

[H]C1(COC([H])(OC2=C(C=C(Br)C=C2)C(=O)NC2=CC=C(Cl)C=C2)C([H])(OC(C)=O)C1([H])OC(C)=O)OC(C)=O

InChIKey

InChIKey=BTHNVHDYRQZPHU-UHFFFAOYSA-N

Formula

C24H23BrClNO9

Mass

584.8

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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 - Benzanilide - Aromatic anilide - O-glycosyl compound - Halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - Tricarboxylic acid or derivatives - Benzoic acid or derivatives - Benzamide - Phenoxy compound - Phenol ether - Benzoyl - Halobenzene - Chlorobenzene - Bromobenzene - Benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Aryl halide - Aryl chloride - Aryl bromide - Secondary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organochloride - Organobromide - Organohalogen compound - Carbonyl group - 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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