CAS 924-44-7
:Ethyl glyoxylate
- Acetic acid, 2-oxo-, ethyl ester
- Acetic acid, oxo-, ethyl ester
- Ethyl 2-Oxoacetate
- Ethyl glyoxylate
- Ethyl oxoacetate
- Ethylglyoxylat
- Formyl ethoxy ketone
- Glioxilato De Etilo
- Glyoxalic acid ethyl ester
- Glyoxylate d'ethyle
- Glyoxylic acid ethyl ester
- Glyoxylsaureethylester
- Nsc 49206
- See more synonyms
Ethyl Glyoxylate Polymer form (47% in Toluene)
CAS:Formula:(CH3CH2OCOCHO)nColor and Shape:Colorless to Almost colorlessclear liquidEthyl glyoxylate, ca 50% soln. in toluene
CAS:Ethyl glyoxylate is widely used as an intermediate in the synthesis of pharmaceuticals (high reactivity of aldehyde function). It is used in the synthesis of a biodegradable polymer, poly(ethyl glyoxylate). It is actively involved in the Friedel-Crafts alkylation reactions with thiophenes to give th
Formula:C4H6O3Color and Shape:Solution, Clear colorless to pale yellowMolecular weight:102.09Ethyl glyoxylate, 50% solution in toluene
CAS:Formula:OHCCO2CH2CH3Purity:≥ 97.0%Color and Shape:Colourless to pale yellow liquidMolecular weight:102.09Ethyl oxoacetate, 50% solution in toluene
CAS:Ethyl oxoacetate, 50% solution in tolueneFormula:C4H6O3Purity:techColor and Shape: clear. almost colourless liquidMolecular weight:102.08864g/molEthyl 2-oxoacetate in 50% Toluene (polymerised)
CAS:Formula:C4H6O3Purity:97.0%Color and Shape:Liquid, OilMolecular weight:102.089Ethyl glyoxalate - 50% in toluene
CAS:Ethyl glyoxalate is a fatty acid that has a hydroxyl group on the second carbon. It is used in palladium-catalyzed coupling reactions to form covalent linkages. This compound has been shown to be an effective antimicrobial agent against amine and ester hydrochloride, as well as being active against several bacteria strains. The asymmetric synthesis of this compound is achieved by reacting diethyl ketomalonate with acetaldehyde in the presence of catalytic quantities of palladium, which leads to formation of two different enantiomers. The reaction mechanism has been elucidated, revealing that the reaction proceeds via a carbonyl addition followed by nucleophilic attack on the ketone oxygen atom. Structural analysis demonstrates that the product formed can be either syn or anti depending on the orientation of reactants during reaction.
Formula:C4H6O3Purity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:102.09 g/molEthyl Glyoxylate-13C4
CAS:Controlled ProductApplications Ethyl Glyoxylate-13C4 is an isotope labelled analog of Ethyl Glyoxylate. Ethyl Glyoxylate is used as a reagent in the synthesis of a new class of cinnamyl-triazole compounds which can be used as selective inhibitors of human aromatase (cytochrome P 450 19A1).
References McNulty, J., et al.: Bioorg. Med. Chem. Lett., 24, 4586 (2014)Formula:C4H6O3Color and Shape:NeatMolecular weight:106.059






