Ethyl potassium malonate
Ethyl potassium malonate
  • CAS No.:6148-64-7
Other grades of this product :
Ethyl potassium malonate Basic information
Product Name:Ethyl potassium malonate
Synonyms:AKOS 310;MALONIC ACID MONOETHYL ESTER POTASSIUM SALT;ETHYL POTASSIUM MALONATE;ETHYL MALONATE MONOPOTASSIUM SALT;ETHYL MALONATE POTASSIUM SALT;ETHYL MONO POTASSIUM MALONATE;KEM;MALONIC ACID MONOETHYL ESTER POTASSIUM
CAS:6148-64-7
MF:C5H9KO4
MW:172.22
EINECS:228-156-7
Product Categories:Pharmaceutical Intermediates;bc0001
Mol File:6148-64-7.mol
Ethyl potassium malonate Chemical Properties
Melting point 194 °C (dec.) (lit.)
storage temp. Inert atmosphere,Room Temperature
solubility Methanol (Slightly), Water (Slightly)
form Powder or Cyrstals
color White
PHpH(50g/l, 25℃) : 5.5~8.0
Water Solubility soluble
Sensitive Hygroscopic
BRN 3721682
InChIKeyWVUCPRGADMCTBN-UHFFFAOYSA-M
CAS DataBase Reference6148-64-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 2
HS Code 29171910
MSDS Information
ProviderLanguage
Ethyl potassium malonate English
SigmaAldrich English
ACROS English
ALFA English
Ethyl potassium malonate Usage And Synthesis
Chemical Propertieswhite crystals or powder
UsesEthyl potassium malonate is used as a competitive inhibitor of the enzyme succinate dehydrogenase. It acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation. Further, it reacts with aryl nitriles to prepare beta-amino acrylates in the presence of zinc chloride and a catalytic amount of Hünig's base. In addition to this, it serves as an intermediate for the preparation of ethyl tert-butyl malonate.
UsesEthyl potassium malonate (potassium ethyl malonate) may be used to generate (trimethylsilyl)ethyl malonate in situ, which can be acylated to prepare a variety of β-ketoesters or alkylidene malonates.
General DescriptionEthyl potassium malonate (potassium ethyl malonate) reacts with aryl nitriles in the presence of zinc chloride and a catalytic amount of Hünig′s base to yield β-amino acrylates. Ethyl potassium malonate is formed as an intermediate during the synthesis of ethyl tert-butyl malonate.

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