79707-53-2 Usage
Uses
Used in Research and Biomedical Applications:
8-(benzyloxy)-2-methylimidazo[1,2-a]pyridine is used as a reference standard in analytical testing for its potential biological activities and properties. It aids in the development and validation of analytical methods and serves as a control in experiments.
Used in Pharmaceutical Development:
8-(benzyloxy)-2-methylimidazo[1,2-a]pyridine may have potential applications in the development of pharmaceuticals due to its unique chemical structure and biological activities. It can be further studied and modified to create new drugs with therapeutic benefits.
Used in Toxicological Studies:
8-(benzyloxy)-2-methylimidazo[1,2-a]pyridine is used in toxicological studies to investigate its role as a mutagen and carcinogen. Understanding its effects on biological systems can help in assessing the safety and potential risks associated with its use in various applications.
Used in Chemical Synthesis:
As a heterocyclic compound, 8-(benzyloxy)-2-methylimidazo[1,2-a]pyridine can be used as a building block or intermediate in the synthesis of other complex organic molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 79707-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,0 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79707-53:
(7*7)+(6*9)+(5*7)+(4*0)+(3*7)+(2*5)+(1*3)=172
172 % 10 = 2
So 79707-53-2 is a valid CAS Registry Number.
79707-53-2Relevant academic research and scientific papers
Antinuclear Agents. 1. Gastric Antisecretory and Cytoprotective Properties of Substituted Imidazopyridines
Kaminski, James J.,Bristol, James A.,Puchalski, Chester,Lovey, Raymond G.,Elliott, Arthur J.,et al.
, p. 876 - 892 (2007/10/02)
A novel class of antinuclear agents, the substituted imidazopyridines, is described.The present compounds are not histamine (H2) receptor antagonists nor are they prostaglandin analoques, yet they exhibit both gastric antisecretory and c