3D-FE55073 - ethyl-44-difluoroacetoacetate
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Ethyl 4,4-difluoroacetoacetate
CAS:Fórmula:C6H8F2O3Pureza:95%Cor e Forma:LiquidPeso molecular:166.1227Ref: IN-DA0037M5
5g21,00€1kg165,00€25g29,00€100g50,00€10kgA consultar25kgA consultar500g127,00€50kgA consultarEthyl 4-chloro-4,4-difluoroacetoacetate
CAS:Ethyl 4-chloro-4,4-difluoroacetoacetatePureza:≥95%Cor e Forma:LiquidPeso molecular:200.57g/molEthyl 2-chloro-4,4-difluoroacetoacetate
CAS:Ethyl 2-chloro-4,4-difluoroacetoacetateFórmula:C6H7ClF2O3Pureza:techCor e Forma: clear liquidPeso molecular:200.57g/molEthyl 4-bromo-4,4-difluoroacetoacetate
CAS:Ethyl 4-bromo-4,4-difluoroacetoacetatePureza:95%Peso molecular:245.02g/molEthyl 4,4-difluoroacetoacetate
CAS:Ethyl 4,4-difluoroacetoacetateFórmula:C6H8F2O3Pureza:97%Cor e Forma: clear. colourless liquidPeso molecular:166.12272g/molEthyl 4,4-Difluoroacetoacetate
CAS:Fórmula:C6H8F2O3Pureza:>96.0%(GC)Cor e Forma:Colorless to Almost colorless clear liquidPeso molecular:166.12Ethyl 2,2-difluoroacetoacetate
CAS:Ethyl 2,2-difluoroacetoacetatePureza:95%Peso molecular:166.12g/molEthyl 4,4-difluoroacetoacetate
CAS:Fórmula:C6H8F2O3Pureza:90%Cor e Forma:Liquid, ClearPeso molecular:166.124Ethyl 4,4-Difluoroacetoacetate
CAS:Produto ControladoApplications Ethyl 4,4-Difluoroacetoacetate is an intermediate used for the synthesis of pharmaceuticals such as potassium channel activators and β-alanine derived GABA-T antagonists.
References Qi, J.L., et al.: Euro. J. Medn. Chem., 46, 934 (2011); Schirlin, D., et al.: J. Enzymes. Inhibition., 1, 243 (1987);Fórmula:C6H8F2O3Cor e Forma:NeatPeso molecular:166.12BUTANOIC ACID, 4-CHLORO-4,4-DIFLUORO-3-OXO, -ETHYL ESTER
CAS:Fórmula:C6H7ClF2O3Pureza:95%Peso molecular:200.5678Ethyl 4-bromo-4,4-difluoro-3-oxobutanoate, Ethyl 4-bromo-4,4-difluoro-3-oxobutyrate
CAS:Fórmula:C6H7BrF2O3Pureza:95%Cor e Forma:LiquidPeso molecular:245.01882,2-Difluoro-3-oxobutyric acid ethyl ester
CAS:2,2-Difluoro-3-oxobutyric acid ethyl ester is an alcohol that is synthesized through a chemoenzymatic process. It is used as a substrate in the reaction with sodium formate and formate dehydrogenase. This synthetic method was developed by E.J. Corey in 1972 and has been used to synthesize optically pure (R)-2,2-difluoro-3-oxobutyric acid ethyl ester. The synthesis of (S)-2,2-difluoro-3-oxobutyric acid ethyl ester can be achieved by using glucose dehydrogenase instead of formate dehydrogenase.Fórmula:C6H8F2O3Pureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:166.12 g/molButanoic acid, 2-(ethoxymethylene)-4,4-difluoro-3-oxo-, ethyl ester
CAS:Fórmula:C9H12F2O4Pureza:98%Cor e Forma:LiquidPeso molecular:222.1860Ethyl 4,4-difluoro-2-(ethoxymethylene)acetoacetate
CAS:Ethyl 4,4-difluoro-2-(ethoxymethylene)acetoacetate
Fórmula:C9H12F2O4Pureza:95%Cor e Forma: clear. colorless liquidPeso molecular:222.19g/mol
