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Methyl ethyl fumaric acid ester, also known as methyl ethyl fumarate, is a chemical compound with the molecular formula C7H10O4. It is an ester derived from fumaric acid, an unsaturated dicarboxylic acid, and is formed by the reaction of fumaric acid with methanol and ethanol. This colorless liquid is soluble in water and has a fruity odor. Methyl ethyl fumarate is commonly used as a flavoring agent in the food and beverage industry, as well as a fragrance component in cosmetics and personal care products. It is also employed as a plasticizer and a solvent in various industrial applications.

4749-70-6

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4749-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4749-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,4 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4749-70:
(6*4)+(5*7)+(4*4)+(3*9)+(2*7)+(1*0)=116
116 % 10 = 6
So 4749-70-6 is a valid CAS Registry Number.

4749-70-6Relevant academic research and scientific papers

Stereoselective Formation of Maleic Acid Diester from Two Diazo Acetic Acid Esters on a Raney Nickel Surface. Evidence for Dipod-chemisorbed Carbenes

Bock, Hans,Wolf, Hans Peter

, p. 690 - 692 (1990)

The N2 elimination from diazo acetic acid esters, heterogeneously catalysed by Raney Nickel, yields as chemidesorbed main product up to 93percent maleic acid diester, cis-stereoselectivity is observed and additional methyl/ethyl ester crossing experiments provide evidence for dipod-chemisorbed surface carbene intermediates.

Synthesis of α,β-unsaturated esters of perfluoropolyalkylethers (PFPAEs) based on hexafluoropropylene oxide units for photopolymerization

Bonneaud, Céline,Decostanzi, Mélanie,Burgess, Julia,Trusiano, Giuseppe,Burgess, Trevor,Bongiovanni, Roberta,Joly-Duhamel, Christine,Friesen, Chadron M.

, p. 32664 - 32671 (2018/10/15)

α,β-unsaturated esters are usually synthesized for polymer applications. However, the addition of maleate (cis-configuration) to a fluorinated moiety is challenging due to its potential isomerization during esterification. Various synthetic routes were attempted and led to very low conversion or side-products. The immiscibility of both reagents combined with an easy isomerization or attack on the double bond were potential explanations. In this paper, the synthesis of maleates oligo(hexafluoropropylene oxide) is reported by Steglich esterification and the reaction conditions are discussed depending on the molecular weight of the fluorinated moieties. After UV-curing, hydrophobic polymers were obtained by copolymerization with vinyl ethers by electron acceptor-donor systems.

Cyclopropanation Catalysed by RuCl2(PPh3)3 and OsCl2(PPh3)3

Demonceau, A.,Lemoine, C. A.,Noels, A. F.,Chizhevsky, I. T.,Sorokin, P.V.

, p. 8419 - 8422 (2007/10/02)

OsCl2(PPh3)3 is a cyclopropanation catalyst using ethyl diazoacetate with a variety of activated alkenes; OsCl2(PPh3)3 is however less active than RuCl2(PPh3)3 for the decomposition of the diazo reagent and the subsequent cyclopropanation.

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