L-Serine, 2-methyl-, methyl ester, hydrochloride

Base Information

Chemical Name:L-Serine, 2-methyl-, methyl ester, hydrochloride
CAS No.:114396-63-3
Molecular Formula:C5H11NO3.ClH
Molecular Weight:169.608
Hs Code.:
Mol file:114396-63-3.mol

Synonyms:α-methylserine methyl ester HCl salt;HCl*H-α-MeSer-OMe;L-Serine, 2-methyl-, methyl ester, hydrochloride;hydrochloride;methyl α-methylserinate hydrochloride;α-methyl-serine methyl ester hydrochloride salt;(S)-2-Amino-3-hydroxy-2-methyl-propionic acid methyl ester;methyl (S)-α-methylserinate;

Suppliers and Price of L-Serine, 2-methyl-, methyl ester, hydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 9 raw suppliers

Chemical Property of L-Serine, 2-methyl-, methyl ester, hydrochloride

Chemical Property:

PSA：72.55000
LogP:0.37140

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses L-Serine, 2-Methyl-, Methyl ester, hydrochloride is a useful research chemical.

Technology Process of L-Serine, 2-methyl-, methyl ester, hydrochloride

There total 5 articles about L-Serine, 2-methyl-, methyl ester, 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: 95.0%

: (2S,4S)-3-tert-butyl 4-methyl 2-tert-butyl-4-methyl-1,3-oxazolidine-3,4-dicarboxylate

: 114396-63-3,134899-86-8
(S)-methyl 2-amino-3-hydroxy-2-methylpropanoate hydrochloride

Guidance literature:: With hydrogenchloride; In water; at 80 ℃;
DOI:10.1002/anie.201801165

Reference yield: 86.0%

: (S)-methyl-2-((((4-chlorobenzyl)oxy)carbonyl)amino)-2-methyl-3-((4-(trifluoromethyl)benzyl)oxy) propanoate

: 114396-63-3,134899-86-8
(S)-methyl 2-amino-3-hydroxy-2-methylpropanoate hydrochloride

Guidance literature:: (S)-methyl-2-((((4-chlorobenzyl)oxy)carbonyl)amino)-2-methyl-3-((4-(trifluoromethyl)benzyl)oxy) propanoate; With palladium 10% on activated carbon; hydrogen; acetic acid; In methanol; at 20 ℃; for 12h; under 760.051 Torr;

With hydrogenchloride; In methanol; diethyl ether;
DOI:10.1080/10286020.2019.1634058