Structure Information
Structure

Compound Identification

SMILES

CCOP(=O)(OCC)C1CC[C@@H](OC1=O)[C@H]1O[C@H]([C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)N1C=CC(NC(C)=O)=NC1=O

InChIKey

InChIKey=RFFCIYSSRLKWIH-YPZJALOJSA-N

Formula

C31H56N3O10PSi2

Mass

717.944

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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

Glycosylamines

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

N-glycosyl compound - N-acetylarylamine - N-arylamide - Dialkyl alkylphosphonate - Pyrimidone - Delta valerolactone - Delta_valerolactone - Phosphonic acid diester - Phosphonic acid ester - Pyrimidine - Hydropyrimidine - Imidolactam - Oxane - Trialkylheterosilane - Oxolane - Heteroaromatic compound - Organophosphonic acid derivative - Acetamide - Silyl ether - Carboxamide group - Lactone - Secondary carboxylic acid amide - Carboxylic acid ester - Carboxylic acid derivative - Organoheterosilane - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Organic metalloid salt - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic metalloid moeity - Carbonyl group - Organonitrogen compound - Organophosphorus compound - Organic oxide - Organosilicon compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).

External Descriptors

Not available

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