DL-Alanine, N-(phenylmethyl)-, ethyl ester

Base Information

Chemical Name:DL-Alanine, N-(phenylmethyl)-, ethyl ester
CAS No.:64892-53-1
Molecular Formula:C12H17NO2
Molecular Weight:207.272
Hs Code.:

Synonyms:

Suppliers and Price of DL-Alanine, N-(phenylmethyl)-, ethyl ester

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of DL-Alanine, N-(phenylmethyl)-, ethyl ester

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of DL-Alanine, N-(phenylmethyl)-, ethyl ester

There total 14 articles about DL-Alanine, N-(phenylmethyl)-, ethyl ester 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: 100.0%

: 100-46-9
benzylamine

: 535-11-5,41978-69-2
Ethyl 2-bromopropionate

: 64892-53-1
N-benzylalanine ethyl ester

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ol402385v

Reference yield: 93.0%

: ethyl 2-[(N-benzyl-N-ethoxycarbonyl)amino]propanoate

: 64892-53-1
N-benzylalanine ethyl ester

Guidance literature:: ethyl 2-[(N-benzyl-N-ethoxycarbonyl)amino]propanoate; With trimethylsilyl iodide; In chloroform; for 24h; Inert atmosphere; Reflux;

With methanol; In chloroform; for 3h; Inert atmosphere; Reflux;
DOI:10.1002/chem.201402514

Reference yield: 84.0%

: 37488-40-7
benzylamine hydrobromide

: 535-11-5,41978-69-2
Ethyl 2-bromopropionate

: 64892-53-1
N-benzylalanine ethyl ester

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 20 - 25 ℃; for 12h; chemoselective reaction; Molecular sieve;
DOI:10.1039/c4ra01915f