58481-17-7 Usage
Uses
Used in Pharmaceutical Research and Development:
2-Hydroxymethyl-isonicotinic acid methyl ester is utilized as a pharmaceutical intermediate for the synthesis of new drugs. Its biological activity, as observed in various assays, makes it a candidate for further exploration and development in the pharmaceutical industry.
Used in Drug Development for Infectious Diseases:
In the field of infectious disease treatment, 2-Hydroxymethyl-isonicotinic acid methyl ester is used as a potential therapeutic agent, particularly for the treatment of tuberculosis. Its potential in this area highlights its importance in the ongoing search for new and effective treatments against this and possibly other infectious diseases.
Used in Safety and Toxicity Studies:
Given its potential for toxicity and reactivity, 2-Hydroxymethyl-isonicotinic acid methyl ester is also used in safety and toxicity studies to ensure that any pharmaceutical products developed using 2-Hydroxymethyl-isonicotinic acid methyl ester meet the necessary safety standards and protocols for human use.
Check Digit Verification of cas no
The CAS Registry Mumber 58481-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,8 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58481-17:
(7*5)+(6*8)+(5*4)+(4*8)+(3*1)+(2*1)+(1*7)=147
147 % 10 = 7
So 58481-17-7 is a valid CAS Registry Number.
58481-17-7Relevant academic research and scientific papers
Atmosphere Dependent Photoreaction of 4-Pyridinecarboxylic Ester in Acidic Methanolic Solutions
Sugiyama, Toru,Kusano, Yukari,Yagi, Kazuya,Ito, Yoko,Sugimori, Akira
, p. 1882 - 1886 (2007/10/02)
The UV-irradiation of methyl 4-pyridinecarboxylate (1) in methanol under oxygen in the presence of sulfuric acid brings about methoxylation at the 3-position of the pyridine ring, while under nitrogen methoxylation and hydroxymethylation occur at the 2-position.The change of photoreactions of 1 caused by oxygen can not be explained either by the promotion of intersystem crossing by O2 or by the charge transfer interactions between 1 and O2.
