Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)[Si](C)(C)[C@@H]1[C@@H](CC(=O)N2CC3=CC=CC=C3C[C@H]2CO)O[C@@]2([C@H]1C)C(=O)N(CC1=CC=C(NC(=O)[C@H]3O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]3O)C=C1)C1=CC=CC=C21

InChIKey

InChIKey=URYBLVLDEHLQQX-MMTABTPTSA-N

Formula

C46H53N3O11Si

Mass

852.025

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Tetrahydroisoquinolines

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Tetrahydroisoquinolines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Tetrahydroisoquinoline - Anilide - Indole or derivatives - Phenol ether - N-arylamide - Phenoxy compound - Methoxybenzene - Anisole - Alkyl aryl ether - Alkylarylsilane - Pyran - Benzenoid - Oxane - Monosaccharide - Monocyclic benzene moiety - Oxolane - Tertiary carboxylic acid amide - Carboxamide group - Hemiacetal - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Polyol - Organic metalloid salt - Azacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Alcohol - Carbonyl group - Organosilicon compound - Primary alcohol - Alkylsilane - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives.

External Descriptors

Not available

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