Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O)C1[C@H]2CC(=O)[C@H](N2C1=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=YBIDYTOJOXKBLO-XIGCLMEMSA-N

Formula

C16H16N2O7

Mass

348.311

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Subclass

Amino acids, peptides, and analogues

Intermediate Tree Nodes

Amino acids and derivatives - Alpha amino acids and derivatives

Direct Parent

Alpha amino acid esters

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Alpha-amino acid ester - Carbapenam - Benzyloxycarbonyl - Nitrobenzene - Nitroaromatic compound - Caprolactam - Oxoproline - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Azepane - Monocyclic benzene moiety - Pyrrolidone - 3-pyrrolidone - 1,3-dicarbonyl compound - Benzenoid - Beta-lactam - Pyrrolidine - Tertiary carboxylic acid amide - Cyclic ketone - Azetidine - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - C-nitro compound - Organic nitro compound - Secondary alcohol - Tertiary amine - Organic oxoazanium - Azacycle - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxide - Organic zwitterion - Organic salt - Organic nitrogen compound - Amine - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

External Descriptors

Not available

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