40334-96-1 Usage
Uses
Used in Pharmaceutical Industry:
2,4-dimethoxy-6-methylpyridine is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
2,4-dimethoxy-6-methylpyridine is used as a precursor in the synthesis of agrochemicals. Its presence in these compounds can contribute to the development of new pesticides or herbicides, enhancing agricultural productivity and crop protection.
Used in Organic Synthesis:
2,4-dimethoxy-6-methylpyridine is used as a versatile intermediate in the synthesis of other organic compounds. Its reactivity and functional groups make it a valuable component in the preparation of complex molecules for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40334-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,3 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40334-96:
(7*4)+(6*0)+(5*3)+(4*3)+(3*4)+(2*9)+(1*6)=91
91 % 10 = 1
So 40334-96-1 is a valid CAS Registry Number.
40334-96-1Relevant academic research and scientific papers
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.
