Compound Identification
SMILES
C\C(NCCN1CCOCC1)=C1\C(=O)NC(=O)N(C2CCCCC2)C1=O
InChIKey
InChIKey=BSSMLAMHCIEADU-FYWRMAATSA-N
Formula
C18H28N4O4
Mass
364.446
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazines
-
Subclass
Pyrimidines and pyrimidine derivatives
-
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 Morpholines Diazinanes Vinylogous amides Dicarboximides Trialkylamines Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Dialkyl ethers Enamines Dialkylamines Hydrocarbon derivatives Carbonyl compounds Organic oxides Organopnictogen compounds
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Barbiturate - N-acyl urea - Ureide - 1,3-diazinane - Morpholine - Oxazinane - Dicarboximide - Vinylogous amide - Amino acid or derivatives - Carbonic acid derivative - Urea - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Oxacycle - Azacycle - Secondary amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Amine - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aliphatic 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