Structure Information
Structure

Compound Identification

SMILES

CNN=C(C1NC(=O)NC1=O)C(=O)NC1=C(C=C(C=C1)[N+]([O-])=O)[N+]([O-])=O

InChIKey

InChIKey=SSGWIGQGYHMDAX-UHFFFAOYSA-N

Formula

C12H11N7O7

Mass

365.262

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Azolidines

Subclass

Imidazolidines

Intermediate Tree Nodes

Imidazolidinones - Imidazolidinediones

Direct Parent

Hydantoins

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - Anilide - Nitrobenzene - Nitroaromatic compound - N-arylamide - 5-monosubstituted hydantoin - Ureide - N-acyl urea - Benzenoid - Monocyclic benzene moiety - Dicarboximide - Organic nitro compound - N-alkylated hydrazone - Urea - Secondary carboxylic acid amide - Carbonic acid derivative - C-nitro compound - Carboxamide group - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Hydrazone - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as hydantoins. These are heterocyclic compounds containing an imidazolidine substituted by ketone group at positions 2 and 4.

External Descriptors

Not available

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