Methyl 3-amino-2-methylpropanoate hydrochloride

Base Information

• Chemical Name: Methyl 3-amino-2-methylpropanoate hydrochloride
• CAS No.: 88512-06-5
• Molecular Formula: C5H11NO2.ClH
• Molecular Weight: 153.609
• European Community (EC) Number: 843-623-0
• DSSTox Substance ID: DTXSID70516966

Synonyms:methyl 3-amino-2-methylpropanoate hydrochloride;88512-06-5;Methyl 3-amino-2-methylpropanoate HCl;Propanoic acid, 3-amino-2-methyl-, methyl ester, hydrochloride;methyl 3-amino-2-methylpropanoate;hydrochloride;MFCD16547718;SCHEMBL2115;DTXSID70516966;RVPWGKBKRYTOHJ-UHFFFAOYSA-N;AKOS026743334;BS-36032;SY184434;CS-0253549;methyl3-amino-2-methylpropanoatehydrochloride;EN300-64705;E72583;methyl 3-amino-2-methyl-propanoate hydrochloride salt;methy 3-amino-2-methylpropionate hydrogen chloride salt;Z1357902409;Methyl 3-amino-2-methylpropanoate--hydrogen chloride (1/1)

Chemical Property of Methyl 3-amino-2-methylpropanoate hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 153.0556563
• Heavy Atom Count: 9
• Complexity: 82.5

Purity/Quality:

98% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CN)C(=O)OC.Cl

Technology Process of Methyl 3-amino-2-methylpropanoate hydrochloride

There total 2 articles about Methyl 3-amino-2-methylpropanoate 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: 90.0%

methanol (67-56-1) + DL-3-aminoisobutyric acid (10569-72-9) → β-aminoisobutyric acid methyl ester hydrochloride (88512-06-5)

Guidance literature:

With thionyl chloride; at 0 - 20 ℃; for 6h;

Reference yield:

DL-3-aminoisobutyric acid (10569-72-9) → β-aminoisobutyric acid methyl ester hydrochloride (88512-06-5)

Guidance literature:

With thionyl chloride; In methanol;

Reference yield: 86.0%

β-aminoisobutyric acid methyl ester hydrochloride (88512-06-5) → 3-amino-2-methyl propan-1-ol (15518-10-2)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 3h; Inert atmosphere; Reflux;

upstream raw materials:

DL-3-aminoisobutyric acid

methanol

Downstream raw materials:

3-amino-2-methyl propan-1-ol

5,6-dihydrothymine

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