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2-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

2-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Structure
  • ₹8227
  • Product name: 2-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • CAS: 118811-03-3
  • MF: C12H23NO3
  • MW: 229.32
  • EINECS:
  • MDL Number:MFCD03701252
  • Synonyms:BOC-2-(2-PIPERIDYL)ETHANOL;2-(2-HYDROXYETHYL)-1-BOC-PIPERIDINE;2-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;1-BOC-2-(2-HYDROXY-ETHYL)-PIPERIDINE;(+/-)-N-BOC-PIPERIDINE-2-ETHANOL;N-BOC-2-HYDROXYETHYLPIPERIDINE;N-BOC-2-(2-HYDROXYETHYL)PIPERIDINE;N-BOC-2-PIPERIDIN-2-YL-ETHANOL
1 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 5G
  • ManufacturerSigma-Aldrich(India)
  • Product number668265
  • Product descriptionN-Boc-2-piperidineethanol 97%
  • Packaging5G
  • Price₹8227
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 668265 N-Boc-2-piperidineethanol 97% 5G ₹8227 2022-06-14 Buy

Properties

Boiling point :100-110 °C/0.3 mmHg
Density :1.032 g/mL at 25 °C
refractive index :n20/D 1.472
Flash point :110 °C
pka :15.15±0.10(Predicted)
CAS DataBase Reference :118811-03-3(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictogramsGHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H301 Toxic if swalloed Acute toxicity,oral Category 3 Danger GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
H400 Very toxic to aquatic life Hazardous to the aquatic environment, acute hazard Category 1 Warning GHS hazard pictograms P273, P391, P501
Precautionary statements:
P273 Avoid release to the environment.

Description

Reactant for synthesis of:
  • Vasopressin1b receptor antagonists
  • CXCR4 antagonists as anti-HIV agents
  • Coumarin-based inhibitors of inducible nitric oxide synthase
  • Selective thrombin inhibitors

Reactant for:
  • N-directed hydroboration for synthesis of amino alcohols
  • Enantioselective synthesis of sedamine and allosedamine

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