(S)-Ethyl 2-aminobutanoate hydrochloride

Base Information

• Chemical Name: (S)-Ethyl 2-aminobutanoate hydrochloride
• CAS No.: 91462-82-7
• Molecular Formula: C₆H₁₃NO₂*ClH
• Molecular Weight: 167.636
• European Community (EC) Number: 965-142-6
• Mol file: 91462-82-7.mol

Synonyms:91462-82-7;(S)-Ethyl 2-aminobutanoate hydrochloride;ethyl (2S)-2-aminobutanoate;hydrochloride;(S)-2-Aminobutyric acid ethyl ester hydrochloride;(S)-2-Aminobutyric acid ethyl ester HCl;SCHEMBL3188318;SWNBPYRQCHSZSE-JEDNCBNOSA-N;Butanoic acid, 2-amino-, ethyl ester, hydrochloride, (2S)-;MFCD11848830;(S)-Ethyl2-aminobutanoatehydrochloride;AKOS015932753;(S)-ETHYL 2-AMINOBUTANOATE HCL;DS-12354;CS-0162057;EN300-7360285;ETHYL (2S)-2-AMINOBUTANOATE HYDROCHLORIDE;(S)-2-Amino-butyric acid ethyl ester hydrochloride;(S)-Ethyl 2-aminobutanoate hydrochloride (H-Abu-OEt.HCl)

Chemical Property of (S)-Ethyl 2-aminobutanoate hydrochloride

Chemical Property:

• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 167.0713064
• Heavy Atom Count: 10
• Complexity: 93.1

Purity/Quality:

99% ^*data from raw suppliers

(S)-Ethyl2-aminobutanoatehydrochloride 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(C(=O)OCC)N.Cl
• Isomeric SMILES: CC[C@@H](C(=O)OCC)N.Cl

Technology Process of (S)-Ethyl 2-aminobutanoate hydrochloride

There total 2 articles about (S)-Ethyl 2-aminobutanoate hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

ethanol (64-17-5) + L-2-aminobutyric acid (1492-24-6) → L-2-aminobutyric acid ethyl ester hydrochloride (91462-82-7)

Guidance literature:

With chloro-trimethyl-silane; at 70 ℃; for 15h;

Reference yield:

C11H21NO4 (1187550-22-6) → L-2-aminobutyric acid ethyl ester hydrochloride (91462-82-7)

Guidance literature:

With hydrogenchloride; water; In 1,4-dioxane;

DOI:10.1016/j.ejmech.2009.04.043

Reference yield: 80.0%

2-iodocyclohex-2-en-1-one (33948-36-6) + L-2-aminobutyric acid ethyl ester hydrochloride (91462-82-7) → (S)-(-)-2-phenylamino-propionic acid ethyl ester (54860-84-3)

Guidance literature:

L-2-aminobutyric acid ethyl ester hydrochloride; With potassium carbonate; In ethanol; at 20 ℃; for 1h; Inert atmosphere;

2-iodocyclohex-2-en-1-one; With toluene-4-sulfonic acid; In ethanol; at 75 ℃; for 6h; Inert atmosphere;

DOI:10.1002/ejoc.201201263

upstream raw materials:

C₁₁H₂₁NO₄

ethanol

L-2-aminobutyric acid

Downstream raw materials:

C₂₃H₃₂N₇O₅P

(S)-(-)-2-phenylamino-propionic acid ethyl ester

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