CAS 763-69-9

Ethyl 3-ethoxypropionate

Description:

Ethyl 3-ethoxypropionate, with the CAS number 763-69-9, is an organic compound classified as an ester. It is characterized by its clear, colorless liquid form and has a pleasant, fruity odor. The molecular structure consists of an ethyl group and a 3-ethoxypropionate moiety, which contributes to its solubility in organic solvents while being less soluble in water. This compound is primarily used as a solvent in various applications, including coatings, paints, and inks, due to its ability to dissolve a wide range of substances. Ethyl 3-ethoxypropionate exhibits moderate volatility and has a relatively low boiling point, making it suitable for use in formulations that require quick drying times. Additionally, it is considered to have low toxicity, but safety precautions should still be observed when handling it, as with any chemical substance. Overall, its unique properties make it valuable in industrial applications, particularly in the formulation of products requiring effective solvent characteristics.

Formula: C₇H₁₄O₃

InChI: InChI=1/C7H14O3/c1-3-9-6-5-7(8)10-4-2/h3-6H2,1-2H3

InChI key: InChIKey=BHXIWUJLHYHGSJ-UHFFFAOYSA-N

SMILES: C(C(OCC)=O)COCC

Synonyms:

• 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
• Ethyl-3-ethoxypropionate
• Ethyl 3-ethoxypropionate
• 4-03-00-00697 (Beilstein Handbook Reference)
• 3-ethoxy-propanoicaciethylester
• beta-Ethoxypropionic acid ethyl ester
• Propanoicacid,3-ethoxy-,ethylester
• 3-ethoxy-propanoicacidethylester
• ethoxypropionicacid,ethylester
• Ethyl 3-ethoxypropionate, 99+%
• 3-ethoxy-propionicaciethylester
• Ektapro EEP Solvent
• ethylesterkyseliny3-ethoxypropionove
• Ethyl ester of 3-ethoxypropanoic acid
• Ethylethoxy propionate

Ethyl 3-Ethoxypropionate

CAS: 763-69-9

Formula: C₇H₁₄O₃

Purity: >99.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 146.19

Ref: 3B-E0319

Ethyl 3-ethoxypropionate, 99+%

CAS: 763-69-9

Ethyl 3-ethoxypropionate is used in the synthesis of phenols and selective inhibitors of cyclin-dependant kinase 4/6 for novel cancer therapies. It is also used as a solvent to prepare polymers. Further, it is used in paints and coatings. This Thermo Scientific Chemicals brand product was originally

Formula: C₇H₁₄O₃

Purity: 99+%

Color and Shape: Clear colorless, Liquid

Molecular weight: 146.19

Ref: 02-B24024

Ethyl 3-Ethoxypropionate

CAS: 763-69-9

Formula: C₇H₁₄O₃

Purity: 97%

Color and Shape: Liquid

Molecular weight: 146.1843

Ref: IN-DA0034UW

Ethyl 3-ethoxypropanoate

CAS: 763-69-9

Ethyl 3-ethoxypropanoate

Purity: 95%

Molecular weight: 146.19g/mol

Ref: 54-OR93689

Ethyl 3-Ethyoxypropionate

CAS: 763-69-9

Ethyl 3-Ethyoxypropionate

Purity: 98%

Molecular weight: 146.18g/mol

Ref: 54-OR1030727

Ethyl 3-ethoxypropionate

CAS: 763-69-9

Formula: C₇H₁₄O₃

Purity: ≥ 99.0%

Color and Shape: Clear, colourless to light yellow liquid

Molecular weight: 146.19

Ref: 7W-GX2541

Ethyl 3-ethoxypropanoate

CAS: 763-69-9

Formula: C₇H₁₄O₃

Purity: 97%

Color and Shape: Liquid

Molecular weight: 146.186

Ref: 10-F462645

Ethyl 3-Ethyoxypropionate

Controlled Product

CAS: 763-69-9

Formula: C₇H₁₄O₃

Color and Shape: Neat

Molecular weight: 146.18

Ref: TR-E917835

Ethyl 3-Ethoxypropionate

CAS: 763-69-9

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.

Formula: C₇H₁₄O₃

Purity: Min. 95%

Molecular weight: 146.19 g/mol

Ref: 3D-AAA76369