14187-25-8 Usage
Description
3-HYDROXY-2,6-DI(HYDROXYMETHYL)PYRRIDINE HYDROCHLORIDE is a pyridine derivative with the molecular formula C7H11NO3Cl. It is a hydrochloride salt of 3-hydroxy-2,6-di(hydroxymethyl)pyridine, known for its mild reducing properties in organic synthesis and potential neuroprotective effects.
Uses
Used in Pharmaceutical and Biochemical Applications:
3-HYDROXY-2,6-DI(HYDROXYMETHYL)PYRRIDINE HYDROCHLORIDE is used as a mild reducing agent in organic synthesis for its ability to facilitate certain chemical reactions, making it a valuable component in the development of pharmaceuticals and biochemical compounds.
Used in Neuroprotection Research:
In the field of neuroscience, 3-HYDROXY-2,6-DI(HYDROXYMETHYL)PYRRIDINE HYDROCHLORIDE is studied for its potential neuroprotective effects, which may contribute to the prevention or treatment of neurodegenerative diseases by protecting neurons from damage or degeneration.
Used in Inhibition of Advanced Glycation End Products:
3-HYDROXY-2,6-DI(HYDROXYMETHYL)PYRRIDINE HYDROCHLORIDE is also being investigated for its ability to inhibit the formation of advanced glycation end products, which are associated with aging and various chronic diseases, including diabetes and Alzheimer's disease.
It is crucial to handle 3-HYDROXY-2,6-DI(HYDROXYMETHYL)PYRRIDINE HYDROCHLORIDE with care, adhering to proper safety procedures and guidelines to ensure the safety of researchers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 14187-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,8 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14187-25:
(7*1)+(6*4)+(5*1)+(4*8)+(3*7)+(2*2)+(1*5)=98
98 % 10 = 8
So 14187-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3.ClH/c9-3-5-1-2-7(11)6(4-10)8-5;/h1-2,9-11H,3-4H2;1H
14187-25-8Relevant articles and documents
Synthesis of pyridine-based polyaminocarboxylic ligands bearing a thioalkyl anchor
Lin, Yi,Favre-Réguillon, Alain,Pellet-Rostaing, Stéphane,Lemaire, Marc
, p. 3463 - 3466 (2008/02/10)
A bicyclic tetraazatriacetic chelating agent containing a thioalkyl pendant group was prepared. Four synthetic routes have been investigated via a Mitsunobu reaction from 2,4-[bishydroxymethyl]-3-hydroxy-pyridine 1. Deprotection of trityl thioether compound 5c led to ligand 6c in 22% overall yield from the starting 3-hydroxypyridine.