5-ethyl-4-hydroxy-2-methylfuran-3(2H)-one

Available forms:YELLOW LIQUID

pd_proNo:225140-67194671-1e0e-49de-ab51-3b2a5a5d4001

pd_productuse:

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Detailed introduction

Offer Chemical Raw Material 5-ethyl-4-hydroxy-2-methylfuran-3(2H)-one 27538-10-9 In Stock

  • Molecular Formula:C7H10O3
  • Molecular Weight:142.155
  • Appearance/Colour:YELLOW LIQUID 
  • Vapor Pressure:0.0121mmHg at 25°C 
  • Refractive Index:n20/D 1.512(lit.)  
  • Boiling Point:231 °C at 760 mmHg 
  • PKA:9.62±0.40(Predicted) 
  • Flash Point:93.5 °C 
  • PSA:46.53000 
  • Density:1.184 g/cm3 
  • LogP:1.54390 

Ethyl furaneol(Cas 27538-10-9) Usage

Preparation

One commercially applied synthesis is the condensation of 2-pentene nitrile with ethyl lactate followed by oxidation of the intermediate 4-cyano-5-ethyl-2-methyldihydro-3(2H)-furanone with monoperoxysulfate.

InChI:InChI=1/C7H10O3/c1-3-5-7(9)6(8)4(2)10-5/h4,9H,3H2,1-2H3

27538-10-9 Relevant articles

Dialkoxydiepoxyalkane: Zur Synthese von 4-Hydroxy-3(2H)-furanonen

Baumann, Manfred,Hoffmann, Werner

, p. 709 (1981)

-

Formation of 4-hydroxy-2,5-dimethyl-3(2H)-furanone and 4-hydroxy-2(or 5)-ethyl-5(or 2)-methyl-3(2H)-furanone through maillard reaction based on pentose sugars

Blank, Imre,Fay, Laurent B.

, p. 531 - 536 (1996)

The caramel-like smelling compounds 4-hy...

Nicotinamide-dependent Ene reductases as alternative biocatalysts for the reduction of activated alkenes

Durchschein, Katharina,Wallner, Silvia,MacHeroux, Peter,Schwab, Wilfried,Winkler, Thorsten,Kreis, Wolfgang,Faber, Kurt

, p. 4963 - 4968 (2013/01/14)

Four NAD(P)H-dependent non-flavin ene re...

Functional characterization of enone oxidoreductases from strawberry and tomato fruit

Klein, Dorothee,Fink, Barbara,Arold, Beate,Eisenreich, Wolfgang,Schwab, Wilfried

, p. 6705 - 6711 (2008/09/17)

Fragaria x ananassa enone oxidoreductase...

Potential of gas chromatography-orthogonal acceleration time-of-flight mass spectrometry (GC-oaTOFMS) in flavor research

Fay, Laurent B.,Newton, Anthony,Simian, Herve,Robert, Fabien,Douce, David,Hancock, Peter,Green, Martin,Blank, Imre

, p. 2708 - 2713 (2007/10/03)

Gas chromatography-orthogonal accelerati...

27538-10-9 Process route

6,7-Dideoxyheptose

6,7-Dideoxyheptose

homofuraneol
27538-10-9

homofuraneol

4-hydroxy-2-methyl-5-ethyl-3-oxo-2H-furan
27538-09-6

4-hydroxy-2-methyl-5-ethyl-3-oxo-2H-furan

Conditions
Conditions Yield
With piperidine; acetic acid; In ethanol; at 80 ℃; for 20h; Yield given. Yields of byproduct given;
homofuraneol
27538-10-9

homofuraneol

4-hydroxy-2-methyl-5-ethyl-3-oxo-2H-furan
27538-09-6

4-hydroxy-2-methyl-5-ethyl-3-oxo-2H-furan

Conditions
Conditions Yield
2.6 g (63%)

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