Record Information
Version 1.0
Update Date 1/22/2018 11:54:54 AM
Metabolite IDPAMDB100040
Identification
Name: 2,4-diacetylphloroglucinol
Description:A benzenetriol that is phloroglucinol in which two of the ring hydrogens are replaced by acetyl groups.
Structure
Thumb
Synonyms:
  • 1,1'-(2,4,6-Trihydroxy-1,3-phenylene)bisethanone
  • 1,5-diacetyl-2,4,6-trihydroxybenzene
  • 1-(3-acetyl-2,4,6-trihydroxyphenyl)ethanone
  • 2,4,6-trihydroxy-1,3-diacetylbenzene
  • 5-acetyl-2,4,6-trihydroxyacetophenone
  • di
Chemical Formula: C10H10O5
Average Molecular Weight: 210.1834
Monoisotopic Molecular Weight: 210.053
InChI Key: PIFFQYJYNWXNGE-UHFFFAOYSA-N
InChI:InChI=1S/C10H10O5/c1-4(11)8-6(13)3-7(14)9(5(2)12)10(8)15/h3,13-15H,1-2H3
CAS number: Not Available
IUPAC Name:1,1'-(2,4,6-trihydroxy-1,3-phenylene)diethanone
Traditional IUPAC Name: Not Available
SMILES:CC(=O)c1c(O)cc(O)c(C(C)=O)c1O
Chemical Taxonomy
Taxonomy DescriptionThis compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
Kingdom Organic compounds
Super ClassOrganic oxygen compounds
Class Organooxygen compounds
Sub ClassCarbonyl compounds
Direct Parent Alkyl-phenylketones
Alternative Parents
Substituents
  • Alkyl-phenylketone
  • Acylphloroglucinol derivative
  • Acetophenone
  • Phloroglucinol derivative
  • Benzenetriol
  • Aryl alkyl ketone
  • Benzoyl
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Benzenoid
  • Monocyclic benzene moiety
  • Vinylogous acid
  • Polyol
  • Hydrocarbon derivative
  • Organic oxide
  • Aromatic homomonocyclic compound
Molecular Framework Aromatic homomonocyclic compounds
External Descriptors
  • methyl ketone, aromatic ketone, benzenetriol, diketone (CHEBI:78688)
Physical Properties
State: Not Available
Charge:0
Melting point: Not Available
Experimental Properties: Not Available
Predicted Properties
PropertyValueSource
Mass210.1828ChemAxon
logP1.2086ChemAxon
H-bond acceptors5ChemAxon
H-bond donors3ChemAxon
Rotatable bonds2ChemAxon
PSA94.8300ChemAxon
RO5 violations0ChemAxon
RO3 violations2ChemAxon
Refractivity52.9000ChemAxon
Atoms25ChemAxon
Rings1ChemAxon
Heavy atoms15ChemAxon
Hydrogen atoms10ChemAxon
Heteroatoms5ChemAxon
N/O atoms5ChemAxon
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:
    • Haas D, Défago G. Biological control of soil-borne pathogens by fluorescent pseudomonads. Nat Rev Microbiol. 2005 Apr;3(4):307-19. Pubmed: 15759041
    Synthesis Reference: Not Available
    Material Safety Data Sheet (MSDS) Not Available
    External Links:
    ResourceLink
    Wikipedia2,4-Diacetylphloroglucinol