(R)-methyl 2-(benzylamino)propanoate

Base Information Edit

Chemical Name:(R)-methyl 2-(benzylamino)propanoate
CAS No.:120571-58-6
Molecular Formula:C11H15NO2
Molecular Weight:193.246
Hs Code.:
European Community (EC) Number:837-157-7
Nikkaji Number:J1.547.072K
Mol file:120571-58-6.mol

Synonyms:(R)-methyl 2-(benzylamino)propanoate;120571-58-6;methyl (2R)-2-(benzylamino)propanoate;BZL-D-ALA-OME HCL;95071-12-8;SCHEMBL914510;N-benzyl D-alanine methyl ester;N-benzyl-D-alanine methyl ester;HIVDOHPKFIBYPZ-SECBINFHSA-N;VEA57158;(R)-methyl2-(benzylamino)propanoate;AKOS022986449;CS-0091534;(R)-2-benzylamino-propionic acid methyl ester;D75153;EN300-204062;(2R)-2-(Benzylamino)propionic acid methyl ester;(2R)-2-Benzylamino-propionic acid methyl ester

Suppliers and Price of (R)-methyl 2-(benzylamino)propanoate

Supply Marketing:Edit

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 3 raw suppliers

Chemical Property of (R)-methyl 2-(benzylamino)propanoate Edit

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:193.110278721
Heavy Atom Count:14
Complexity:176

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)OC)NCC1=CC=CC=C1
Isomeric SMILES:C[C@H](C(=O)OC)NCC1=CC=CC=C1

Technology Process of (R)-methyl 2-(benzylamino)propanoate

There total 18 articles about (R)-methyl 2-(benzylamino)propanoate 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%

: 120571-58-6
N-benzyl D-alanine methyl ester

Guidance literature:: With sodium tris(acetoxy)borohydride; triethylamine; In 1,2-dichloro-ethane; at 20 ℃; Molecular sieve; Inert atmosphere;

Reference yield: 91.0%

: 14316-06-4
D-alanine methyl ester hydrochloride

: 100-52-7
benzaldehyde

: 120571-58-6
N-benzyl D-alanine methyl ester

Guidance literature:: D-alanine methyl ester hydrochloride; benzaldehyde; With triethylamine; In tetrahydrofuran; at 20 ℃; for 48h;

With sodium tetrahydroborate; In methanol; at 0 ℃; for 3h;