Compound Identification
SMILES
OCCCN\C=C1\C(=O)NC(=O)N(CC2=CC=CC=C2)C1=O
InChIKey
InChIKey=IUYCTACRDXLMDU-XFXZXTDPSA-N
Formula
C15H17N3O4
Mass
303.318
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazines
-
Subclass
Pyrimidines and pyrimidine derivatives
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Level 5
Pyrimidones
- Level 6 Barbituric acid derivatives
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Level 5
Pyrimidones
-
Subclass
Pyrimidines and pyrimidine derivatives
-
Class
Diazines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazines
Subclass
Pyrimidines and pyrimidine derivatives
Intermediate Tree Nodes
Pyrimidones
Direct Parent
Barbituric acid derivatives
Alternative Parents
N-acyl ureas Benzene and substituted derivatives Diazinanes 1,3-aminoalcohols Vinylogous amides Dicarboximides Amino acids and derivatives Enamines Dialkylamines Allylamines Azacyclic compounds Primary alcohols Carbonyl compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Barbiturate - N-acyl urea - Ureide - Monocyclic benzene moiety - 1,3-diazinane - Benzenoid - Vinylogous amide - 1,3-aminoalcohol - Dicarboximide - Urea - Amino acid or derivatives - Carbonic acid derivative - Azacycle - Alkanolamine - Allylamine - Secondary amine - Carboxylic acid derivative - Secondary aliphatic amine - Enamine - Organic oxide - Alcohol - Organic oxygen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic nitrogen compound - Primary alcohol - Amine - Hydrocarbon derivative - Organopnictogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as barbituric acid derivatives. These are compounds containing a perhydropyrimidine ring substituted at C-2, -4 and -6 by oxo groups.
External Descriptors
Not available