2-Piperidinecarboxylicacid,4-hydroxy-,methylester,(2S,4R)-(9CI)

Base Information

Chemical Name:2-Piperidinecarboxylicacid,4-hydroxy-,methylester,(2S,4R)-(9CI)
CAS No.:211058-80-9
Molecular Formula:C7H13NO3
Molecular Weight:159.185
Hs Code.:
Mol file:211058-80-9.mol

Synonyms:2-Piperidinecarboxylicacid,4-hydroxy-,methylester,(2S,4R)-(9CI);(2S,4R)-4-Hydroxy-2-piperidinecarboxylic acid methyl ester;(2S,4R)-Methyl-4-hydroxypiperidine-2-carboxylate

Suppliers and Price of 2-Piperidinecarboxylicacid,4-hydroxy-,methylester,(2S,4R)-(9CI)

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

TRC
(2S,4R)-Methyl-4-hydroxypiperidine-2-carboxylate
10mg
$ 165.00

TRC
(2S,4R)-Methyl-4-hydroxypiperidine-2-carboxylate
100mg
$ 1320.00

Medical Isotopes, Inc.
(2S,4R)-Methyl-4-hydroxypiperidine-2-carboxylate
25 mg
$ 650.00

Total 3 raw suppliers

Chemical Property of 2-Piperidinecarboxylicacid,4-hydroxy-,methylester,(2S,4R)-(9CI)

Chemical Property:

PSA：58.56000
LogP:-0.39890

Purity/Quality:

98%Min ^*data from raw suppliers

(2S,4R)-Methyl-4-hydroxypiperidine-2-carboxylate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses (2S,4R)-Methyl-4-hydroxypiperidine-2-carboxylate has been used as a reactant for the preparation of cholecystokinin B (CCK-B) antagonists.

Technology Process of 2-Piperidinecarboxylicacid,4-hydroxy-,methylester,(2S,4R)-(9CI)

There total 8 articles about 2-Piperidinecarboxylicacid,4-hydroxy-,methylester,(2S,4R)-(9CI) 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%

: 403503-37-7,1357348-22-1
(2S,4R)-1-benzyl 2-methyl 4-hydroxypiperidine-1,2-dicarboxylate

: 211058-80-9,189952-45-2
methyl 4(R)-hydroxypiperidine-2(S)-carboxylate

Guidance literature:: With palladium on activated charcoal; hydrogen; In ethanol; at 20 ℃; for 16h;
DOI:10.1016/j.bmcl.2015.09.009

Reference yield: 99.0%

: 254882-06-9,181269-87-4
(2S,4R)-methyl 1-(tert-butoxycarbonyl)-4-hydroxypiperidine-2-carboxylate

: 211058-80-9,189952-45-2
methyl 4(R)-hydroxypiperidine-2(S)-carboxylate

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 10h;

Reference yield: 98.0%

: 1103929-22-1
methyl (2S,4R)-4-hydroxy-1-((R)-1-phenylethyl)piperidine-2-carboxylate

: 211058-80-9,189952-45-2
methyl 4(R)-hydroxypiperidine-2(S)-carboxylate

Guidance literature:: With palladium(II) hydroxide/carbon; palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 2h;
DOI:10.1016/j.bmcl.2008.08.083