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(=CC=C1)N1C=CC=C(OC)C1=O)C1=C2C=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=IZARVFXHQHLSPM-ABXIKWSZSA-N

Formula

C46H48N4O9Si

Mass

828.994

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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 - Indole or derivatives - Phenoxy compound - Nitroaromatic compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Dihydropyridine - Pyridinone - Alkylarylsilane - Monocyclic benzene moiety - Hydropyridine - Pyridine - Benzenoid - Oxolane - Heteroaromatic compound - Tertiary carboxylic acid amide - Carboxamide group - Lactam - C-nitro compound - Organic nitro compound - Organic metalloid salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Organic oxoazanium - Oxacycle - Azacycle - Organic zwitterion - Hydrocarbon derivative - Organic nitrogen compound - Organic salt - Organic metalloid moeity - Alcohol - Organonitrogen compound - Organooxygen compound - Organosilicon compound - Alkylsilane - Primary alcohol - Organic oxygen compound - Carbonyl group - Organic oxide - 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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