Structure Information
Structure

Compound Identification

SMILES

CC1=CN(C2OC(CO[Si](C)(C)C(C)(C)C)C3(OS(=O)(=O)C=C3N)C2O[Si](C)(C)C(C)(C)C)C(=O)N(CC(=O)N(CCCl)CCCl)C1=O

InChIKey

InChIKey=AXEHIZQONAEJGX-UHFFFAOYSA-N

Formula

C30H52Cl2N4O9SSi2

Mass

771.9

Export to:

JSON SDF CSV

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 heteropolycyclic compounds

Substituents

N-glycosyl compound - Nitrogen mustard - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Sulfonic acid ester - Organosulfonic acid ester - Heteroaromatic compound - Vinylogous amide - Tertiary carboxylic acid amide - Trialkylheterosilane - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - 1,2-oxathiole - Oxolane - Carboxamide group - Silyl ether - Lactam - Urea - Tertiary amine - Amino acid or derivatives - Organic metalloid salt - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Enamine - Organoheterosilane - Alkyl halide - Primary aliphatic amine - Organosilicon compound - Alkyl chloride - Organic nitrogen compound - Carbonyl group - Organic oxide - Organohalogen compound - Organic metalloid moeity - Organochloride - Organonitrogen compound - Hydrocarbon derivative - Amine - Aromatic heteropolycyclic 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

Previous Back Next