Methyl 3-(methylamino)propanoate hydrochloride

Base Information

• Chemical Name: Methyl 3-(methylamino)propanoate hydrochloride
• CAS No.: 65103-50-6
• Molecular Formula: C₅H₁₁NO₂*ClH
• Molecular Weight: 153.609
• European Community (EC) Number: 854-569-2

Synonyms:65103-50-6;methyl 3-(methylamino)propanoate hydrochloride;Methyl 3-(methylamino)propanoate HCl;N-Methyl-b-alanine methyl ester HCl;methyl 3-(methylamino)propanoate;hydrochloride;b-Alanine, N-methyl-, methyl ester, hydrochloride;SCHEMBL380895;GYJOTTXQHSJQOF-UHFFFAOYSA-N;MFCD08456671;AB11809;BS-32674;methyl N-methyl-beta-alaninate hydrochloride;methyl3-(methylamino)propanoatehydrochloride;CS-0454555;FT-0702642;EN300-1702697

Chemical Property of Methyl 3-(methylamino)propanoate hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 153.0556563
• Heavy Atom Count: 9
• Complexity: 72.8

Purity/Quality:

95%-98% ^*data from raw suppliers

Methyl3-(methylamino)propanoatehydrochloride 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CNCCC(=O)OC.Cl

Technology Process of Methyl 3-(methylamino)propanoate hydrochloride

There total 2 articles about Methyl 3-(methylamino)propanoate 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: 46.0%

methanol (67-56-1) + N-(2-cyanoethyl)-N-methylamine (693-05-0) → methyl 3-(N-methylamino)propionate hydrochloride (65103-50-6)

Guidance literature:

With hydrogenchloride; sodium sulfate; at 20 ℃; for 5h;

DOI:10.1021/jm9000693

Reference yield:

methyl 3-(N-tert-butoxycarbonyl-N-methyl)-aminopropionate (119740-95-3) → methyl 3-(N-methylamino)propionate hydrochloride (65103-50-6)

Guidance literature:

With hydrogenchloride; In ethyl acetate; at 20 ℃;

DOI:10.1248/cpb.51.759

Reference yield:

2-fluoro-4-{5-[2-(methoxymethyl)-2'-methylbiphenyl-4-yl]-1,2,4-oxadiazol-3-yl}benzoyl chloride (1141475-56-0) + methyl 3-(N-methylamino)propionate hydrochloride (65103-50-6) → C29H28FN3O5

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃;

DOI:10.1002/cmdc.201402557

upstream raw materials:

methyl 3-(N-tert-butoxycarbonyl-N-methyl)-aminopropionate

methanol

N-(2-cyanoethyl)-N-methylamine

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