Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[Si](OC[C@@H](O)[C@H]1OC(=O)[C@H](OS(=O)(=O)C(F)(F)F)[C@H](O)[C@H]1OCC1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1

InChIKey

InChIKey=UHYXHOZTJPOFRI-JQPIIJRMSA-N

Formula

C31H35F3O9SSi

Mass

668.75

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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

Monosaccharides - Hexoses

Direct Parent

Gluconolactones

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Gluconolactone - Benzylether - Trifluoromethanesulfonate - Alkylarylsilane - Delta_valerolactone - Delta valerolactone - Oxane - Sulfonic acid ester - Organosulfonic acid ester - Monocyclic benzene moiety - Benzenoid - Methanesulfonate - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Secondary alcohol - Silyl ether - Lactone - Trihalomethane - Carboxylic acid ester - Organoheterosilane - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organic metalloid salt - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Alcohol - Alkyl halide - Hydrocarbon derivative - Halomethane - Organic oxide - Carbonyl group - Organosilicon compound - Alkyl fluoride - Organohalogen compound - Organic metalloid moeity - Organofluoride - Organosulfur compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as gluconolactones. These are polyhydroxy acids containing a gluconolactone molecule, which is characterized by a tetrahydropyran substituted by three hydroxyl groups, one ketone group, and one hydroxymethyl group.

External Descriptors

Not available

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