2-Methyl-1,3-cyclopentanedione

2-Methyl-1,3-cyclopentanedione
  • CAS No.:765-69-5
Other grades of this product :
2-Methyl-1,3-cyclopentanedione Basic information
Product Name:2-Methyl-1,3-cyclopentanedione
Synonyms:2-Methyl-1,3-cyclopentadione;2-METHYLCYCLOPENTAN-1,3-DIONE;2-METHYL-1,3-CYCLOPENTANEDIONE;METHYLCYCLE-D;2-Methylcyclopentane-1,3-dione,98%;1,3-Cyclopentanedione, 2-methyl-;2-METHYL-1,3-CYCLOPENTANEDIONE(METHYLCYCLO-D);2-Methyl-1,3-cyclopentanediolne
CAS:765-69-5
MF:C6H8O2
MW:112.13
EINECS:212-153-2
Product Categories:Miscellaneous;ketone;C3 to C6;Carbonyl Compounds;Ketones
Mol File:765-69-5.mol
2-Methyl-1,3-cyclopentanedione Chemical Properties
Melting point 212-215 °C (lit.)
Boiling point 213°C (estimate)
density 1.0795 (rough estimate)
refractive index 1.4550 (estimate)
storage temp. Store below +30°C.
solubility Solubility in hot Methanol (almost transparency).
pka10.83±0.20(Predicted)
form Crystalline Powder
color Light beige to tan
PH2.95 at 24.7℃ and 10g/L
BRN 1237255
InChIKeyHXZILEQYFQYQCE-UHFFFAOYSA-N
LogP-0.8 at 30℃ and pH7.66
CAS DataBase Reference765-69-5(CAS DataBase Reference)
NIST Chemistry Reference1,3-Cyclopentanedione, 2-methyl-(765-69-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
Hazard Note Irritant
HS Code 29142900
MSDS Information
ProviderLanguage
2-Methylcyclopentane-1,3-dione English
SigmaAldrich English
ACROS English
ALFA English
2-Methyl-1,3-cyclopentanedione Usage And Synthesis
Chemical PropertiesLIGHT BEIGE TO TAN CRYSTALLINE POWDER
Uses2-Methyl-1,3-cyclopentanedione was used as a reactant in the identification and characterization of benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases.
Uses2-Methyl-1,3-cyclopentanedione hs been used to explore deoxycholic acid (DCA) induced changes in cell signaling. DCA is a secondary bile acid implicated in numerous pathological conditions. It has also been used in the synthesis of (-)-curcumanolide A and (-)-curcumalactone by aldol-lactonization.
Synthesis Reference(s)Synthetic Communications, 19, p. 373, 1989 DOI: 10.1080/00397918908050676

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