Compound Identification
SMILES
FC(F)C(F)(F)COS(=O)(=O)CCC1C(=O)NC(=O)NC1=O
InChIKey
InChIKey=YFUZPMBLVVPHJQ-UHFFFAOYSA-N
Formula
C9H10F4N2O6S
Mass
350.24
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 Sulfonic acid esters Organosulfonic acid esters Diazinanes 1,3-dicarbonyl compounds Sulfonyls Dicarboximides Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Barbiturate - N-acyl urea - Ureide - 1,3-diazinane - Sulfonic acid ester - Organosulfonic acid ester - 1,3-dicarbonyl compound - Dicarboximide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Urea - Carbonic acid derivative - Azacycle - Carboxylic acid derivative - Alkyl halide - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organosulfur compound - Organopnictogen compound - Organic oxygen compound - Alkyl fluoride - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - 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