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53422-71-2

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53422-71-2 Usage

General Description

2-(3,4,5,6-tetrahydropyridin-2-yl)pyridine is a chemical compound with a molecular formula C11H14N2. It is a heterocyclic compound consisting of two linked pyridine rings, with one of the rings containing a tetrahydropyridine moiety. It is commonly used in organic synthesis and chemical research as a building block in the construction of more complex organic molecules. The compound may also have potential applications in medicinal chemistry and pharmaceutical research due to its unique structure and properties. However, further studies and research are needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 53422-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53422-71:
(7*5)+(6*3)+(5*4)+(4*2)+(3*2)+(2*7)+(1*1)=102
102 % 10 = 2
So 53422-71-2 is a valid CAS Registry Number.

53422-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4,5,6-Tetrahydropyridin-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 2-(2,3,4,5-tetrahydropyridin-6-yl)pyridine

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:53422-71-2 SDS

53422-71-2Relevant articles and documents

Synthesis and kinetic resolution of N-Boc-2-arylpiperidines

Cochrane, Edward J.,Leonori, Daniele,Hassall, Lorraine A.,Coldham, Iain

supporting information, p. 9910 - 9913 (2014/08/18)

The chiral base n-BuLi/(-)-sparteine or n-BuLi/(+)-sparteine surrogate promotes kinetic resolution of N-Boc-2-arylpiperidines by asymmetric deprotonation. The enantioenriched starting material was recovered with yields 39-48% and ers up to 97:3. On lithiation then electrophilic quench, 2,2-disubstituted piperidines were obtained with excellent yields and enantioselectivities.

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