Methyl (2E)-4-[(tert-butoxycarbonyl)amino]-5-phenyl-2-pentenoate

Base Information

Chemical Name:Methyl (2E)-4-[(tert-butoxycarbonyl)amino]-5-phenyl-2-pentenoate
CAS No.:115650-05-0
Molecular Formula:C17H23 N O4
Molecular Weight:305.374
Hs Code.:
Mol file:115650-05-0.mol

Synonyms:2-Pentenoicacid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-phenyl-, methyl ester, (E)-(9CI); 2-Pentenoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-phenyl-,methyl ester, (E)-(?à)-

Suppliers and Price of Methyl (2E)-4-[(tert-butoxycarbonyl)amino]-5-phenyl-2-pentenoate

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 2 raw suppliers

Chemical Property of Methyl (2E)-4-[(tert-butoxycarbonyl)amino]-5-phenyl-2-pentenoate

Chemical Property:

PSA：64.63000
LogP:3.24250

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Methyl (2E)-4-[(tert-butoxycarbonyl)amino]-5-phenyl-2-pentenoate

There total 5 articles about Methyl (2E)-4-[(tert-butoxycarbonyl)amino]-5-phenyl-2-pentenoate 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: 67.0%

: 103127-53-3
N-tert-butyloxycarbonyl-2-amino-3-phenylpropionaldehyde

: 96-32-2
bromoacetic acid methyl ester

: 115650-05-0
Methyl (E)-4-((N-tert-butoxycarbonyl)amino)-5-phenyl-2-pentenoate

Guidance literature:: With 1,2,2,3,4,4-hexamethylphosphetane 1-oxide; phenylsilane; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 25 ℃; for 48h; stereoselective reaction;
DOI:10.1021/acscatal.9b02456

Reference yield:

: 51987-73-6,77119-84-7,19901-50-9
methyl 2-tert-butoxycarbonylamino-3-phenylpropanoate

: 115650-05-0
Methyl (E)-4-((N-tert-butoxycarbonyl)amino)-5-phenyl-2-pentenoate

Guidance literature:: With diisobutylaluminium hydride; In methanol; hexane; ethyl acetate; toluene;

Reference yield:

: 4-tert-Butoxycarbonylamino-5-phenyl-2-(pyridin-2-ylsulfanyl)-pentanoic acid methyl ester

: 115650-05-0
Methyl (E)-4-((N-tert-butoxycarbonyl)amino)-5-phenyl-2-pentenoate

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction; 1) chloroform, room temperature, 1h, 2) toluene, 110 deg C, reflux, 1h;
DOI:10.1016/S0040-4020(01)90305-9