Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=NC(C)=C(S1)S(=O)(=O)NC(=O)NC1NC(=O)NC1=O

InChIKey

InChIKey=RANVZQMBNCSASQ-UHFFFAOYSA-N

Formula

C10H12N6O6S2

Mass

376.36

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Azolidines

Subclass

Imidazolidines

Intermediate Tree Nodes

Imidazolidinones - Imidazolidinediones - Hydantoins

Direct Parent

Allantoins

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Allantoin - Alpha-amino acid or derivatives - N-acetylarylamine - 2,4,5-trisubstituted 1,3-thiazole - 5-monosubstituted hydantoin - N-arylamide - N-acyl urea - Sulfonylurea - Ureide - Azole - Dicarboximide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiazole - Heteroaromatic compound - Aminosulfonyl compound - Acetamide - Secondary carboxylic acid amide - Carbonic acid derivative - Urea - Carboxamide group - Carboxylic acid derivative - Azacycle - Organopnictogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as allantoins. These are heterocyclic compounds containing an imiazolidine ring substituted by a ketone group at positions 2 and 5, and an urea at position 4.

External Descriptors

Not available

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