Tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate

Base Information

Chemical Name:Tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate
CAS No.:118811-03-3
Molecular Formula:C12H23NO3
Molecular Weight:229.32
Hs Code.:2933399090
European Community (EC) Number:625-395-2
DSSTox Substance ID:DTXSID00408360
Nikkaji Number:J1.518.626G
Mol file:118811-03-3.mol

Synonyms:118811-03-3;Tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate;N-Boc-2-piperidineethanol;1-Boc-2-(2-hydroxy-ethyl)-piperidine;N-BOC-2-PIPERIDIN-2-YL-ETHANOL;2-(2-Hydroxy-ethyl)-piperidine-1-carboxylic acid tert-butyl ester;1-Piperidinecarboxylicacid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester;MFCD03701252;MFCD02683201;1-Boc-2-(2-hydroxyethyl)piperidine;1-Boc-2-piperidineethanol;N-Boc-2-piperidine ethanol;tert-Butyl2-(2-hydroxyethyl)piperidine-1-carboxylate;F2184-0204;SCHEMBL1551631;DTXSID00408360;LTVQOFUGXMVESU-UHFFFAOYSA-N;N-Boc-2-piperidineethanol, 97%;AMY21735;(+/-)-n-boc-piperidine-2-ethanol;N-Boc-2-(2-hydroxymethyl)piperidine;1-Boc-2-(2-hydroxyethyl)-piperidine;2-(2-Hydroxyethyl)-1-Boc-piperidine;AKOS005263817;AB12455;AB12456;SB31588;AS-36769;SY060236;SY109625;BB 0263066;CS-0075718;FT-0654446;FT-0655617;FT-0659994;EN300-61979;VU0494861-1;1-t-butoxycarbonyl-2-(2-hydroxyethyl)piperidine;J-003890;t-butyl 2-(2-hydroxyethyl)-1-piperidinecarboxylate;N-t-Butoxycarbonyl-2(R,S)-(2-hydroxyethyl)piperidine;tert-Butyl (R)-2-(2-Hydroxyethyl)piperidine-1-carboxylate;tert-BUTOXYCARBONYL-2(R/S)-(2-HYDROXYETHYL)-PIPERIDINE;2-(2-hydroxyethyl)-piperidine-1-carboxylic acid tert-butyl ester;2-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester;1-piperidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester, (2r)-

Suppliers and Price of Tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate

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

Usbiological
N-Boc-2-hydroxyethylpiperidine
2g
$ 333.00

TRC
N-Boc-2-hydroxyethyl-piperazine
100mg
$ 60.00

Sigma-Aldrich
N-Boc-2-piperidineethanol 97%
5g
$ 142.00

Matrix Scientific
tert-Butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate 95%+
1g
$ 101.00

Matrix Scientific
tert-Butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate 95%+
5g
$ 323.00

Matrix Scientific
tert-Butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate 95%+
2.500g
$ 215.00

J&W Pharmlab
1-Boc-2-(2-hydroxy-ethyl)-piperidine 98%
100g
$ 282.00

Crysdot
tert-Butyl2-(2-hydroxyethyl)piperidine-1-carboxylate 97%
500g
$ 850.00

Biosynth Carbosynth
N-Boc-2-hydroxyethylpiperidine
25 g
$ 321.00

Biosynth Carbosynth
N-Boc-2-hydroxyethylpiperidine
10 g
$ 200.00

Total 35 raw suppliers

Chemical Property of Tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate

Chemical Property:

Vapor Pressure:6.34E-06mmHg at 25°C
Refractive Index:n20/D 1.472
Boiling Point:324.066 °C at 760 mmHg
PKA:15.15±0.10(Predicted)
Flash Point:149.79 °C
PSA：49.77000
Density:1.043 g/cm³
LogP:2.09630
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:229.16779360
Heavy Atom Count:16
Complexity:235

Purity/Quality:

97% ^*data from raw suppliers

N-Boc-2-hydroxyethylpiperidine ^*data from reagent suppliers

Safty Information:

Pictogram(s): T
Hazard Codes:T
Statements: 25
Safety Statements: 24/25-45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)N1CCCCC1CCO
Uses Reactant for synthesis of:Vasopressin1b receptor antagonistsCXCR4 antagonists as anti-HIV agentsCoumarin-based inhibitors of inducible nitric oxide synthaseSelective thrombin inhibitorsReactant for: N-directed hydroboration for synthesis of amino alcoholsEnantioselective synthesis of sedamine and allosedamine

Technology Process of Tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate

There total 12 articles about Tert-butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate 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%