123811-72-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Methylpicolinic acid hydrochloride is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds, contributing to the development of new drugs.
Used in Neurodegenerative Disease Treatment:
In the medical field, 3-Methylpicolinic acid hydrochloride is utilized as a potential therapeutic agent for the treatment of neurodegenerative diseases, due to its studied effects on related conditions.
Used as an Enzyme Inhibitor:
3-Methylpicolinic acid hydrochloride serves as an inhibitor of certain enzymes, playing a role in regulating biological processes and potentially offering therapeutic benefits.
Used in Antioxidant Drug Development:
Recognized for its antioxidant properties, 3-Methylpicolinic acid hydrochloride is employed in the development of drugs aimed at managing oxidative stress-related conditions, thereby providing a novel approach to treating associated health issues.
Used in Materials Science:
In the realm of materials science, 3-Methylpicolinic acid hydrochloride has been investigated for its potential use in the fabrication of organic light-emitting diodes and other electronic devices, showcasing its versatility beyond pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 123811-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,8,1 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123811-72:
(8*1)+(7*2)+(6*3)+(5*8)+(4*1)+(3*1)+(2*7)+(1*2)=103
103 % 10 = 3
So 123811-72-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO2.ClH/c1-5-3-2-4-8-6(5)7(9)10;/h2-4H,1H3,(H,9,10);1H
123811-72-3Relevant academic research and scientific papers
An Improved Synthesis of Homoproline and Derivatives
Shuman, Robert T.,Ornstein, Paul L.,Paschal, Jonathan W.,Gesellchen, Paul D.
, p. 738 - 741 (2007/10/02)
An improved, general synthesis of substituted homoprolines has been developed by using readily available substituted pyridines (1).A key step in this synthetic procedure involves the known conversion of pyridine-N-oxides to 2-cyanopyridines (3) in nearly quantitative yields.The resulting nitriles are hydrolyzed to the corresponding pyridine-2-carboxylic acids (4).Subsequent reduction of the aromatic ring with PtO2/H2 gives the homoprolines (5) in good yields as racemic cis isomers.This procedure also can be utilized for the preparation of 5,6-benzohomoprolines fromthe appropriate quinoline precursors.The N-tert-butyloxycarbonyl (Boc) derivatives of these amino acids (useful intermediates for peptide synthesis) were also prepared in good yields.
