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Butanoic acid, 4-bromo-2-[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S)-

Base Information Edit
  • Chemical Name:Butanoic acid, 4-bromo-2-[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S)-
  • CAS No.:15159-67-8
  • Molecular Formula:C13H16BrNO4
  • Molecular Weight:330.178
  • Hs Code.:
  • Mol file:15159-67-8.mol
Butanoic acid, 4-bromo-2-[[(phenylmethoxy)carbonyl]amino]-, methyl
ester, (2S)-

Synonyms:L-Methyl-benzyloxycarbonyl-L-α-amino-γ-brombutyrat;(L)-methyl 2-benzyloxycarbonylamino-4-bromobutanoate;4-Brom-2-carbobenzyloxyamino-buttersaeuremethylester;(S)-2-benzyloxycarbonylamino-4-bromobutyric acid methyl ester;benzyl (S)-1-(methoxycarbonyl)-3-bromopropylcarbamate;(S)-2-benzyloxycarbonylamino-4-bromo-butyric acid methyl ester;

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Chemical Property of Butanoic acid, 4-bromo-2-[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S)- Edit
Chemical Property:
  • Melting Point:61 °C 
  • Boiling Point:444.5±45.0 °C(Predicted) 
  • PSA:64.63000 
  • Density:1.410±0.06 g/cm3(Predicted) 
  • LogP:2.63030 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of Butanoic acid, 4-bromo-2-[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S)-

There total 16 articles about Butanoic acid, 4-bromo-2-[[(phenylmethoxy)carbonyl]amino]-, methyl ester, (2S)- 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:
Guidance literature:
(S)-2-benzyloxycarbonylamino-succinic acid 1-methyl ester; With chloroformic acid ethyl ester;
With sodium tetrahydroborate; In methanol;
With carbon tetrabromide; triphenylphosphine;
DOI:10.1016/S0040-4039(03)01222-X
Guidance literature:
With carbon tetrabromide; In dichloromethane; at 0 - 20 ℃; for 2.5h;
DOI:10.1021/acs.jmedchem.5b00933
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