Ethyl 3-Ethoxypropionate

CAS: 763-69-9

Ref. 3D-AAA76369

Produktinformation

• Name: Ethyl 3-Ethoxypropionate
• Synonyme: 3-Ethoxypropanoic acid ethyl ester, 3-Ethoxypropionate d'ethyle, 3-Ethoxypropionic acid ethyl ester, 3-Etoxipropionato De Etilo, Ai3-03254, Beta-Aethoxypropionsaeure-Aethylester, Bis-(2-Ethoxy)ethyl peroxydicarbonate, Brn 1751976, EEP, Ektapro EEP, Ethoxypropionic acid, ethyl ester, Ethyl 3-ethoxypropanoate, Ethyl 4-oxahexanoate, Ethyl Ethoxypropionate, Ethyl beta-ethoxypropionate, Ethyl β-ethoxypropionate, Ethyl-3-ethoxypropionat, Ethylester kyseliny 3-ethoxypropionove, Ethylester kyseliny 3-ethoxypropionove [Czech], Nsc 8870, Powerblox SV 33, Propanoic acid, 3-ethoxy-, ethyl ester, Propionate, 3-Ethoxy-, Ethyl, Propionic acid, 3-ethoxy-, ethyl ester, Sankio EEP, Solfine EP, Ucar Ester EEP, β-Ethoxypropionic acid ethyl ester
• CAS: 763-69-9

Beschreibung

Ethyl 3-ethoxypropionate is a cycloaddition product of ethyl 3-ethoxypropanoate. It has been shown to be more chemically stable than the reactants and has an increased uptake in the reaction solution.
Ethyl 3-ethoxypropionate is able to undergo a cycloaddition process with diethyl succinate under conditions of high temperature and pressure, leading to the formation of methyl ethyl malonic acid. This chemical reaction takes place via an intermolecular hydrogen bonding interaction between the ethoxy group on one molecule and the ester group on the other molecule. The cyclohexane ring on each molecule also forms a hydrogen bonding interaction with its corresponding methyl or ethyl groups. Ethyl 3-ethoxypropionate is not reactive in its pure form but can undergo reactions when exposed to chemicals such as potassium hydroxide, which leads to its degradation into propionic acid and ethanol.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 146.19 g/mol
• Formel: C₇H₁₄O₃
• Reinheit: Min. 95%