2,6-Dihydroxyacetophenone

Common Name

2,6-Dihydroxyacetophenone Description

Potential component of FEMA 3662. 2,6-Dihydroxyacetophenone is a flavouring ingredient2,6-Dihydroxyacetophenone belongs to the family of Acetophenones. These are organic compounds containing the acetophenone structure. Structure

MOLSDFPDBSMILESInChI

Structure for HMDB29660 (2',6'-Dihydroxyacetophenone)

Synonyms

Value Source 26-Dihydroxy acetophenoneChEMBL 2'6'-DihydroxyacetophenoneChEMBL 26-DihydroxyacetophenoneChEMBL 1-(2,6-Dihydroxyphenyl)-ethanoneHMDB 1-(2,6-Dihydroxyphenyl)ethanoneHMDB 1-(2,6-Dihydroxyphenyl)ethanone, 9ciHMDB 2',6'-Dihydroxy-acetophenoneHMDB 2, 6-DihydroxyacetophenoneHMDB 2,6-DihydroxyacetophenoneHMDB 2-Acetyl-1,3-benzenediolHMDB 2-Acetyl-1,3-dihydroxybenzeneHMDB 2-Acetyl-resorcinolHMDB 2-AcetylresorcinolHMDB Acetophenone, 2',6'-dihydroxy- (8ci)HMDB Acetyl-2,6-dihydroxybenzeneHMDB Ethanone, 1-(2,6-dihydroxyphenyl)- (9ci)HMDB gamma-ResacetophenoneHMDB laquo gammaraquo -ResacetophenoneHMDB

Chemical Formlia

C8H8O3 Average Molecliar Weight

152.1473 Monoisotopic Molecliar Weight

152.047344122 IUPAC Name

1-(2,6-dihydroxyphenyl)ethan-1-one Traditional Name

1-(2,6-dihydroxyphenyl)ethanone CAS Registry Number

699-83-2 SMILES

CC(=O)C1=C(O)C=CC=C1O

InChI Identifier

InChI=1S/C8H8O3/c1-5(9)8-6(10)3-2-4-7(8)11/h2-4,10-11H,1H3

InChI Key

YPTJKHVBDCRKNF-UHFFFAOYSA-N Chemical Taxonomy Description

This compound belongs to the class of organic compounds known as acetophenones. These are organic compounds containing the acetophenone structure. Kingdom

Organic compounds Super Class

Benzenoids Class

Benzene and substituted derivatives Sub Class

Acetophenones Direct Parent

Acetophenones Alternative Parents

  • Resorcinols
  • Benzoyl derivatives
  • Aryl alkyl ketones
  • Vinylogous acids
  • Hydrocarbon derivatives
  • Substituents

  • Acetophenone
  • Aryl alkyl ketone
  • Aryl ketone
  • Resorcinol
  • Benzoyl
  • Phenol
  • Vinylogous acid
  • Ketone
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aromatic homomonocyclic compound
  • Molecliar Framework

    Aromatic homomonocyclic compounds External Descriptors

    Not Available Ontology Status

    Expected but not Quantified Origin

  • Endogenous
  • Food
  • Biofunction

    Not Available Application

  • Flavoring Agent
  • Cellliar locations

  • Cytoplasm
  • Extracellliar
  • Physical Properties State

    Not Available Experimental Properties

    Property Value Reference Melting Point155 – 156 °CNot Available Boiling PointNot AvailableNot Available Water SolubilityNot AvailableNot Available LogPNot AvailableNot Available

    Predicted Properties

    Property Value Source Water Solubility8.84 mg/mLALOGPS logP1.26ALOGPS logP2.22ChemAxon logS-1.2ALOGPS pKa (Strongest Acidic)9.98ChemAxon pKa (Strongest Basic)-3.9ChemAxon Physiological Charge0ChemAxon Hydrogen Acceptor Count3ChemAxon Hydrogen Donor Count2ChemAxon Polar Surface Area57.53 Å2ChemAxon Rotatable Bond Count1ChemAxon Refractivity40.42 m3·mol-1ChemAxon Polarizability14.72 Å3ChemAxon Number of Rings1ChemAxon Bioavailability1ChemAxon Rlie of FiveYesChemAxon Ghose FilterYesChemAxon Vebers RlieYesChemAxon MDDR-like RlieYesChemAxon

    Spectra Spectra

    Spectrum Type Description Splash Key LC-MS/MS

    LC-MS/MS Spectrum – LC-ESI-TOF , negativesplash10-0pbi-0900000000-339591e82b6f9e9fd3afView in MoNA LC-MS/MS

    LC-MS/MS Spectrum – LC-ESI-TOF , negativesplash10-0pbi-0900000000-339591e82b6f9e9fd3afView in MoNA LC-MS/MS

    LC-MS/MS Spectrum – LC-ESI-TOF , negativesplash10-0a4r-0900000000-d7933852722676de249bView in MoNA LC-MS/MS

    LC-MS/MS Spectrum – LC-ESI-TOF , negativesplash10-0a4r-0900000000-d7933852722676de249bView in MoNA LC-MS/MS

    LC-MS/MS Spectrum – LC-ESI-TOF , negativesplash10-0udi-0900000000-bbc9d0fbc313d0295c5fView in MoNA LC-MS/MS

    LC-MS/MS Spectrum – LC-ESI-TOF , negativesplash10-0udi-0900000000-bbc9d0fbc313d0295c5fView in MoNA Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, PositiveNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 10V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 20V, NegativeNot Available Predicted LC-MS/MS

    Predicted LC-MS/MS Spectrum – 40V, NegativeNot Available

    Biological Properties Cellliar Locations

  • Cytoplasm
  • Extracellliar
  • Biofluid Locations

    Not Available Tissue Location

    Not Available Pathways

    Not Available Normal Concentrations Not Available Abnormal Concentrations

    Not Available Associated Disorders and Diseases Disease References

    None Associated OMIM IDs

    None External Links DrugBank ID

    Not Available DrugBank Metabolite ID

    Not Available Phenol Explorer Compound ID

    Not Available Phenol Explorer Metabolite ID

    Not Available FoodDB ID

    FDB000834 KNApSAcK ID

    Not Available Chemspider ID

    62888 KEGG Compound ID

    Not Available BioCyc ID

    Not Available BiGG ID

    Not Available Wikipedia Link

    Not Available NuGOwiki Link

    HMDB29660 Metagene Link

    HMDB29660 METLIN ID

    Not Available PubChem Compound

    69687 PDB ID

    Not Available ChEBI ID

    559127

    Product: PF-915275

    References Synthesis Reference Not Available Material Safety Data Sheet (MSDS) Not Available General References
    1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

    PMID: 27188793