(4-Hydroxy-piperidin-1-yl)-acetic acid tert-butyl ester

Base Information

Chemical Name:(4-Hydroxy-piperidin-1-yl)-acetic acid tert-butyl ester
CAS No.:166955-02-8
Molecular Formula:C₁₁H₂₁NO₃
Molecular Weight:215.293
Hs Code.:
DSSTox Substance ID:DTXSID801244229

Synonyms:166955-02-8;(4-hydroxy-piperidin-1-yl)-acetic acid tert-butyl ester;tert-Butyl 2-(4-hydroxypiperidin-1-yl)acetate;SCHEMBL572705;PJFODMSLPDZJRR-UHFFFAOYSA-N;DTXSID801244229;AKOS009036176;CS-0447924;1,1-Dimethylethyl 4-hydroxy-1-piperidineacetate;A1-01270;(4-hydroxy-piperidin-1-yl)-aceticacidtert-butylester

Suppliers and Price of (4-Hydroxy-piperidin-1-yl)-acetic acid tert-butyl 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

Matrix Scientific
(4-Hydroxy-piperidin-1-yl)-aceticacidtert-butylester
1g
$ 400.00

Matrix Scientific
(4-Hydroxy-piperidin-1-yl)-aceticacidtert-butylester
5g
$ 1200.00

A1 Biochem Labs
(4-Hydroxy-piperidin-1-yl)-aceticacidtert-butylester 95%
5 g
$ 600.00

A1 Biochem Labs
(4-Hydroxy-piperidin-1-yl)-aceticacidtert-butylester 95%
1 g
$ 200.00

Total 1 raw suppliers

Chemical Property of (4-Hydroxy-piperidin-1-yl)-acetic acid tert-butyl ester

Chemical Property:

Boiling Point:311.2±27.0 °C(Predicted)
Density:1.067±0.06 g/cm3(Predicted)
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:215.15214353
Heavy Atom Count:15
Complexity:214

Purity/Quality:: (4-Hydroxy-piperidin-1-yl)-aceticacidtert-butylester ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)CN1CCC(CC1)O

Technology Process of (4-Hydroxy-piperidin-1-yl)-acetic acid tert-butyl ester

There total 3 articles about (4-Hydroxy-piperidin-1-yl)-acetic acid tert-butyl 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: 47.0%