Structure Information
Structure

Compound Identification

SMILES

OCCNC(=O)CN1C=CN=C1[N+]([O-])=O

InChIKey

InChIKey=WCDWBPCFGJXFJZ-UHFFFAOYSA-N

Formula

C7H10N4O4

Mass

214.181

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic nitrogen compounds

Class

Organonitrogen compounds

Subclass

Amines

Intermediate Tree Nodes

Alkanolamines - 1,2-aminoalcohols

Direct Parent

N-acylethanolamines

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Nitroaromatic compound - N-acylethanolamine - N-substituted imidazole - Azole - Imidazole - Heteroaromatic compound - Carboxamide group - C-nitro compound - Secondary carboxylic acid amide - Organic nitro compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organic oxoazanium - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Alcohol - Primary alcohol - Organic oxygen compound - Carbonyl group - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as n-acylethanolamines. These are compounds containing an N-acyethanolamine moiety, which is characterized by an acyl group is linked to the nitrogen atom of ethanolamine.

External Descriptors

CHEBI:75473 : C-nitro compound - monocarboxylic acid amide - imidazoles

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