Record Information
Version 1.0
Update Date 1/22/2018 11:54:54 AM
Metabolite IDPAMDB100009
Identification
Name: acetylpyruvic acid
Description:A dioxo monocarboxylic acid that is pentanoic acid carrying two oxo groups at positions 2 and 4.
Structure
Thumb
Synonyms:
  • 2,4-Dioxopentanoate
  • 2,4-dioxovaleric acid
  • Acetylpyruvate
  • Acetylpyruvic acid
Chemical Formula: C5H6O4
Average Molecular Weight: 130.09874
Monoisotopic Molecular Weight: 130.027
InChI Key: UNRQTHVKJQUDDF-UHFFFAOYSA-N
InChI:InChI=1S/C5H6O4/c1-3(6)2-4(7)5(8)9/h2H2,1H3,(H,8,9)
CAS number: Not Available
IUPAC Name:2,4-dioxopentanoic acid
Traditional IUPAC Name: Not Available
SMILES:CC(=O)CC(=O)C(O)=O
Chemical Taxonomy
Taxonomy DescriptionThis compound belongs to the class of organic compounds known as 3-acylpyruvic acids. These are compounds containing a pyruvic acid substituted at the 3-position by an acyl group.
Kingdom Organic compounds
Super ClassOrganic acids and derivatives
Class Keto acids and derivatives
Sub ClassGamma-keto acids and derivatives
Direct Parent 3-Acylpyruvic acids
Alternative Parents
Substituents
  • 3-acylpyruvic acid
  • 1,3-diketone
  • Short-chain keto acid
  • Alpha-keto acid
  • 1,3-dicarbonyl compound
  • Alpha-hydroxy ketone
  • Ketone
  • Carboxylic acid derivative
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Organic oxygen compound
  • Organooxygen compound
  • Hydrocarbon derivative
  • Carbonyl group
  • Organic oxide
  • Aliphatic acyclic compound
Molecular Framework Aliphatic acyclic compounds
External Descriptors
  • dioxo monocarboxylic acid, beta-diketone (CHEBI:2424)
Physical Properties
State: Not Available
Charge:0
Melting point: Not Available
Experimental Properties: Not Available
Predicted Properties
PropertyValueSource
Mass130.0985ChemAxon
logP-0.3808ChemAxon
H-bond acceptors4ChemAxon
H-bond donors1ChemAxon
Rotatable bonds3ChemAxon
PSA71.4400ChemAxon
RO5 violations0ChemAxon
RO3 violations2ChemAxon
Refractivity28.3208ChemAxon
Atoms15ChemAxon
Rings0ChemAxon
Heavy atoms9ChemAxon
Hydrogen atoms6ChemAxon
Heteroatoms4ChemAxon
N/O atoms4ChemAxon
Inorganic atoms0ChemAxon
Halogen atoms0ChemAxon
Chiral centers0ChemAxon
R/S chiral centers0ChemAxon
Unknown chiral centers0ChemAxon
Undefined chiral centers0ChemAxon
Stereo double bonds0ChemAxon
Cis/trans stereo double bonds0ChemAxon
Unknown stereo double bonds0ChemAxon
Undefined stereo double bonds 0ChemAxon
Biological Properties
Cellular Locations: Not Available
Reactions:
Pathways:
    Spectra
    Spectra: Not Available
    References
    References:
    • Chapman PJ, Ribbons DW. Metabolism of resorcinylic compounds by bacteria: orcinol pathway in Pseudomonas putida. J Bacteriol. 1976 Mar;125(3):975-84. Pubmed: 1254564
    Synthesis Reference: Not Available
    Material Safety Data Sheet (MSDS) Not Available
    External Links:
    ResourceLink
    KEGG COMPOUNDC02132