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39945-50-1

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39945-50-1 Usage

General Description

1-CBZ-2-(2-HYDROXY-ETHYL)-PIPERIDINE is a chemical compound that belongs to the piperidine class of organic compounds. It is a derivative of piperidine with a carboxybenzyl (CBZ) protecting group attached to the nitrogen atom. The molecule also contains a 2-hydroxyethyl group attached to the piperidine ring. 1-CBZ-2-(2-HYDROXY-ETHYL)-PIPERIDINE has potential applications in organic synthesis and pharmaceutical research. It may also be used as a building block in the synthesis of other organic compounds. Additionally, it has properties that make it suitable for use as a reagent in chemical reactions and as a precursor in the synthesis of various pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 39945-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,4 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39945-50:
(7*3)+(6*9)+(5*9)+(4*4)+(3*5)+(2*5)+(1*0)=161
161 % 10 = 1
So 39945-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO3/c17-11-9-14-8-4-5-10-16(14)15(18)19-12-13-6-2-1-3-7-13/h1-3,6-7,14,17H,4-5,8-12H2

39945-50-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-CBZ-2-(2-HYDROXY-ETHYL)-PIPERIDINE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:39945-50-1 SDS

39945-50-1Relevant articles and documents

METHYL OXAZOLE OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 45, (2016/06/28)

The present invention is directed to methyl oxazole compounds which are antagonists of orexin receptors. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.

Non-nucleoside inhibitors of the measles virus RNA-dependent RNA polymerase: Synthesis, structure-activity relationships, and pharmacokinetics

Ndungu, J. Maina,Krumm, Stefanie A.,Yan, Dan,Arrendale, Richard F.,Reddy, G. Prabhakar,Evers, Taylor,Howard, Randy,Natchus, Michael G.,Saindane, Manohar T.,Liotta, Dennis C.,Plemper, Richard K.,Snyder, James P.,Sun, Aiming

supporting information; experimental part, p. 4220 - 4230 (2012/06/30)

The measles virus (MeV), a member of the paramyxovirus family, is an important cause of pediatric morbidity and mortality worldwide. In an effort to provide therapeutic treatments for improved measles management, we previously identified a small, non-nucl

Remote Stereocenter Discrimination in the Enzymatic Resolution of Piperidine-2-ethanol. Short Enantioselective Synthesis of Sedamine and Allosedamine

Angoli, Marco,Barilli, Alessio,Lesma, Giordano,Passarella, Daniele,Riva, Sergio,Silvani, Alessandra,Danieli, Bruno

, p. 9525 - 9527 (2007/10/03)

Kinetic resolution of N-Boc-piperidine-2-ethanol (2), a case of remote stereocenter discrimination, was accomplished by sequential transesterification mediated by two enzymes, Lipase PS and porcine pancreatic lipase, showing opposite enantioselectivity. The gram-scale availability of the two enantiomeric N-Boc alcohols 2a (R) and 2c (S) enlarges their synthetic exploitation for the enantioselective preparation of piperidine alkaloids. As an example, the convenient three-step synthesis of both the enantiomers of sedamine and allosedamine is described.

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