Compound Identification
SMILES
OC1NC(=O)NC(=O)C1(F)N1C=C(F)C(=O)NC1=O
InChIKey
InChIKey=NLAFMRFXDRRFSK-UHFFFAOYSA-N
Formula
C8H6F2N4O5
Mass
276.156
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
Halopyrimidines N-acyl ureas Aryl fluorides Diazinanes Hydropyrimidines Vinylogous amides Dicarboximides Heteroaromatic compounds Fluorohydrins Lactams Alkanolamines Azacyclic compounds Organofluorides Alkyl fluorides Organopnictogen compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Barbiturate - Halopyrimidine - N-acyl urea - Ureide - Aryl fluoride - Aryl halide - 1,3-diazinane - Hydropyrimidine - Dicarboximide - Heteroaromatic compound - Vinylogous amide - Urea - Fluorohydrin - Halohydrin - Carbonic acid derivative - Lactam - Carboxylic acid derivative - Alkanolamine - Azacycle - Organohalogen compound - Organofluoride - Organonitrogen compound - Organic oxide - Alkyl halide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Alkyl fluoride - Organooxygen 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