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(S)-2-(PIPERIDIN-2-YL)PYRIDINE, with the molecular formula C11H14N2, is a pyridine derivative known for its IUPAC name 2-(piperidin-2-yl)pyridine. This chiral compound is a key player in the pharmaceutical industry, recognized for its role as an intermediate in the synthesis of drugs and active pharmaceutical ingredients (APIs). Its structural attributes make it a valuable building block in the creation of heterocyclic compounds and a versatile reagent in organic chemistry reactions. (S)-2-(PIPERIDIN-2-YL)PYRIDINE's potential applications in medicinal chemistry and drug discovery underscore its importance in pharmaceutical research and development.

46041-69-4

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46041-69-4 Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-(PIPERIDIN-2-YL)PYRIDINE is used as a synthetic intermediate for the development of various drugs and active pharmaceutical ingredients (APIs), leveraging its unique structural properties to enhance the therapeutic efficacy of medications.
Used in Medicinal Chemistry:
(S)-2-(PIPERIDIN-2-YL)PYRIDINE is utilized as a building block in the synthesis of heterocyclic compounds, which are integral to the design of novel pharmaceutical agents with diverse biological activities.
Used in Organic Chemistry Reactions:
(S)-2-(PIPERIDIN-2-YL)PYRIDINE serves as a reagent in organic chemistry, contributing to the advancement of chemical processes and the synthesis of complex organic molecules for various applications, including drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 46041-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,0,4 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 46041-69:
(7*4)+(6*6)+(5*0)+(4*4)+(3*1)+(2*6)+(1*9)=104
104 % 10 = 4
So 46041-69-4 is a valid CAS Registry Number.

46041-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-(2'-piperidinyl)pyridine

1.2 Other means of identification

Product number -
Other names (S)-2-(2-piperidinyl)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 -
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More Details:46041-69-4 SDS

46041-69-4Downstream Products

46041-69-4Relevant academic research and scientific papers

Chiral ligand 2-(2′-piperidinyl)pyridine: synthesis, resolution and application in asymmetric diethylzinc addition to aldehydes

Cheng, Yan-Qin,Bian, Zheng,Kang, Chuan-Qing,Guo, Hai-Quan,Gao, Lian-Xun

, p. 1572 - 1575 (2008)

Chiral ligand 2-(2′-piperidinyl)pyridine 1 has been synthesized in good overall yield by sequential benzylation, hydrogenation and debenzylation of 2,2′-bipyridine. Its enantiomerically pure enantiomers have been obtained by resolution of 2-(1-benzyl-2-piperidinyl)pyridine 2 with d-tartaric acid (or l-tartaric acid) followed by debenzylation. The absolute configuration was determined by X-ray analysis of the (S)-2 d-tartrate. It was demonstrated that 1 can be used as an effective enantioselective catalyst in the addition of diethylzinc to aldehydes. Optically active secondary alcohols with up to 100% enantiomeric excess were obtained in high yields.

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