872036-41-4 Usage
Uses
Used in Pharmaceutical Research:
(S)-(-)-4-chloro-2-(1-hydroxyethyl)pyridine is used as an intermediate in the synthesis of various pharmaceuticals for [application reason] its ability to be a part of the development of new drug molecules.
Used in Agrochemical Synthesis:
(S)-(-)-4-chloro-2-(1-hydroxyethyl)pyridine is used as an intermediate in the synthesis of various agrochemicals for [application reason] its role in creating compounds that can be utilized in the agricultural industry.
Used in Chiral Ligand and Catalyst Preparation:
(S)-(-)-4-chloro-2-(1-hydroxyethyl)pyridine is used as a building block for chiral ligands and catalysts for [application reason] the presence of the hydroxyethyl group, which is essential for the preparation of these compounds.
Used in Organic Synthesis:
(S)-(-)-4-chloro-2-(1-hydroxyethyl)pyridine is used as a versatile building block for the synthesis of diverse functionalized pyridine derivatives for [application reason] the chloro group in the compound, which allows for further functionalization and the creation of a wide range of pyridine-based compounds.
Used in Drug Discovery:
(S)-(-)-4-chloro-2-(1-hydroxyethyl)pyridine is used in drug discovery for [application reason] its potential in the development of new drug molecules, contributing to the advancement of pharmaceutical research and the creation of novel therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 872036-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,0,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 872036-41:
(8*8)+(7*7)+(6*2)+(5*0)+(4*3)+(3*6)+(2*4)+(1*1)=164
164 % 10 = 4
So 872036-41-4 is a valid CAS Registry Number.
872036-41-4Relevant articles and documents
Biocatalytic preparation of optically active 4-(N,N-dimethylamino)pyridines for application in chemical asymmetric catalysis
Busto, Eduardo,Gotor-Fernandez, Vicente,Gotor, Vicente
, p. 1007 - 1016 (2006)
4-Chloro-2-(1-hydroxybenzyl)pyridine and 4-chloro-2-(1-hydroxyalkyl)pyridines were obtained with moderate to excellent enantiomeric excesses and high isolated yields by bioreduction with Baker's yeast of the corresponding ketones. The resulting optically active alcohols were transformed into adequate DMAP derivatives, which have been applied in asymmetric catalytic processes as nucleophilic catalysts in the stereoselective chemical alkoxycarbonylation of 1-phenylethanol or as chiral ligands in the enantioselective addition of diethylzinc to benzaldehyde.
