72918-10-6 Usage
Description
2-Methoxy-6-methylnicotinic acid is a chemical compound with the molecular formula C9H9NO4. It belongs to the class of nicotinic acids, which are derivatives of pyridine. 2-Methoxy-6-methylnicotinic acid is characterized by the presence of a methoxy group and a methyl group on the nicotinic acid backbone, giving it unique structural features and potential applications.
Uses
Used in Pharmaceutical Industry:
2-Methoxy-6-methylnicotinic acid is used as a potential drug candidate for targeting nicotinic acid receptors. Its unique structure allows it to interact with these receptors, which may lead to the development of new therapeutic agents for various conditions.
Used in Drug Development:
2-Methoxy-6-methylnicotinic acid is used as a starting point for the development of new drugs. Its potential biological activities and therapeutic properties make it a promising candidate for further research and development in the pharmaceutical industry.
Used in Biological Research:
2-Methoxy-6-methylnicotinic acid is used as a research tool to study the effects of nicotinic acid receptor modulation. Its unique structure and potential interactions with these receptors make it a valuable compound for understanding the underlying mechanisms of action and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 72918-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,1 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72918-10:
(7*7)+(6*2)+(5*9)+(4*1)+(3*8)+(2*1)+(1*0)=136
136 % 10 = 6
So 72918-10-6 is a valid CAS Registry Number.
72918-10-6Relevant articles and documents
Displacement of Protomeric Equilibria by Self-Association: Hydroxypyridine-Pyridone and Mercaptopyridine-Thiopyridone Isomer Pairs
Beak, Peter,Covington, Johnny B.,Smith, Stanley G.,White, J. Matthew,Zeigler, John M.
, p. 1354 - 1362 (2007/10/02)
Values of both self-association and protomeric equilibrium constants are reported for 2-hydroxypyridine-2-pyridone, 4-hydroxypyridine-4-pyridone, and 2-mercaptopyridine-2-thiopyridone isomer pairs in different solvents.These results provide quantitative evidence for significant differences in the positions of protomeric equilibria for self-associated and monomeric species.The 2-substituted isomers are associated as well-known dimers while the 4-substituted systems form oligomers.In polar and hydrogen-bonding solvents self-association is substantially reduced.Sterically hindered 2- and 4-pyridones are less associated than unhindered systems.The implication of these results, that determinations and interpretations of protomeric equilibrium should take into account the possible dominance of self-association, is discussed.
