Ethyl 2-aminopropanoate hydrochloride
Ethyl 2-aminopropanoate hydrochloride Basic information
- Product Name:
- Ethyl 2-aminopropanoate hydrochloride
- Synonyms:
-
- (DL-Alanina ethyl ester hydrochloride
- ETHYL 2-AMINOPROPANOATE HCl
- DL-Alanine ethyl ester hydrochloride≥ 99% (Assay)
- l 2-aminopropanoate hydrochloride
- DL-Ala-OEt·HCl
- Methisosildenafil Impurity 7
- Alanine, ethyl ester,hydrochloride (1:1)
- [(2R)-1-ethoxy-1-oxopropan-2-yl]ammonium
- CAS:
- 617-27-6
- MF:
- C5H12ClNO2
- MW:
- 153.61
- EINECS:
- 210-507-0
- Product Categories:
-
- Alanine [Ala, A]
- Amino Acids 13C, 2H, 15N
- Amino Acids & Derivatives
- Inhibitors
- Alanine
- Amino Acid Derivatives
- Peptide Synthesis
- bc0001
- Mol File:
- 617-27-6.mol
Ethyl 2-aminopropanoate hydrochloride Chemical Properties
- Melting point:
- 85-87 °C(lit.)
- storage temp.
- Inert atmosphere,2-8°C
- solubility
- Methanol (Sparingly), Water
- form
- Granular Powder and Granules
- color
- White
- Sensitive
- Hygroscopic
- BRN
- 3654425
- InChI
- InChI=1S/C5H11NO2.ClH/c1-3-8-5(7)4(2)6;/h4H,3,6H2,1-2H3;1H
- InChIKey
- JCXLZWMDXJFOOI-UHFFFAOYSA-N
- SMILES
- C(=O)(C(N)C)OCC.Cl
- CAS DataBase Reference
- 617-27-6(CAS DataBase Reference)
- EPA Substance Registry System
- Alanine, ethyl ester, hydrochloride (617-27-6)
MSDS
- Language:English Provider:Ethyl 2-aminopropanoate hydrochloride
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
Ethyl 2-aminopropanoate hydrochloride Usage And Synthesis
Chemical Properties
White Crystalline Solid
Uses
Alanine derivative
reaction suitability
reaction type: solution phase peptide synthesis
Synthesis
64-17-5
302-72-7
617-27-6
The general procedure for the synthesis of ethyl 2-aminopropionate hydrochloride from ethanol and DL-alanine was as follows: commercially available DL-alanine (5.00 g, 56.12 mmol) was dissolved in 150 mL of anhydrous ethanol, 5 mL of 37% concentrated hydrochloric acid was added, and the mixture was refluxed for 5 hours. After completion of the reaction, the solvent was removed by evaporation and the resulting colorless oily residue was vacuum dried to give the target product in 92% yield. The product was characterized by 1H NMR (CDCl3): δ 1.05 (t, 3H, J=7.07Hz, -OCH2CH3), 1.45 (d, 3H, J=7.25Hz, -CHCH3), 3.48 (q, 2H, J=7.07Hz, -OCH2CH3), and 4.02 ppm (q, 1H, J=7.25Hz, - CHCH3). High-resolution mass spectrometry (HRMS, ESI, 140 eV) analysis showed that the m/z [M+H+] calculated value for C5H12NO2 was 118.0868 and the measured value was 118.0794.
References
[1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1994, # 7, p. 1455 - 1462
[2] Dalton Transactions, 2008, # 13, p. 1689 - 1697
[3] Polyhedron, 2014, vol. 67, p. 520 - 528
[4] Scientia Pharmaceutica, 2001, vol. 69, # 4, p. 329 - 350
[5] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 6, p. 2336 - 2350
Ethyl 2-aminopropanoate hydrochloride Preparation Products And Raw materials
Raw materials
Preparation Products
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Ethyl 2-aminopropanoate hydrochloride(617-27-6)Related Product Information
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