N-BOC-(S)-isoserine methyl ester

Base Information

Chemical Name:N-BOC-(S)-isoserine methyl ester
CAS No.:133153-76-1
Molecular Formula:C9H17NO5
Molecular Weight:219.238
Hs Code.:
DSSTox Substance ID:DTXSID001152371
Mol file:133153-76-1.mol

Synonyms:133153-76-1;N-BOC-(S)-isoserine methyl ester;methyl (2S)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate;Propanoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxy-, methyl;Methyl (S)-3-((tert-butoxycarbonyl)amino)-2-hydroxypropanoate;methyl (2S)-3-{[(tert-butoxy)carbonyl]amino}-2-hydroxypropanoate;Methyl (S)-3-(Boc-amino)-2-hydroxypropanoate;SCHEMBL7403514;N-BOC-(S)-isoserinemethylester;DQTVOWNRRLNDEY-LURJTMIESA-N;DTXSID001152371;AC8942;CS-0105321;EN300-7045991;(S)-methyl 3-((tert-butoxycarbonyl)amino)-2-hydroxypropanoate;Methyl (2S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxypropanoate

Suppliers and Price of N-BOC-(S)-isoserine methyl ester

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

AK Scientific
N-BOC-(S)-isoserinemethylester
5g
$ 863.00

Total 3 raw suppliers

Chemical Property of N-BOC-(S)-isoserine methyl ester

Chemical Property:

PSA：84.86000
LogP:0.43590
XLogP3:0.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:219.11067264
Heavy Atom Count:15
Complexity:233

Purity/Quality:

98%min ^*data from raw suppliers

N-BOC-(S)-isoserinemethylester ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCC(C(=O)OC)O
Isomeric SMILES:CC(C)(C)OC(=O)NC[C@@H](C(=O)OC)O

Technology Process of N-BOC-(S)-isoserine methyl ester

There total 6 articles about N-BOC-(S)-isoserine methyl 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: 98.0%