98279-50-6 Usage
Uses
Used in Pharmaceutical Industry:
1-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde is used as a key intermediate for the synthesis of various drugs, including calcium channel blockers and antihypertensive agents. Its role in the development of these medications is vital due to its reactivity and structural properties that facilitate the creation of therapeutically relevant compounds.
Used in Agricultural Chemicals:
In the agricultural sector, 1-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde is utilized in the production of pesticides and other agricultural chemicals. Its application in this industry is attributed to its chemical properties that allow for the creation of effective and targeted pest control solutions.
Used in Organic Synthesis:
1-methyl-6-oxo-1,6-dihydropyridine-3-carbaldehyde is also used as a versatile building block in organic synthesis. Its capacity to undergo multiple chemical reactions makes it an essential component in the creation of a wide array of organic compounds for various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 98279-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,7 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98279-50:
(7*9)+(6*8)+(5*2)+(4*7)+(3*9)+(2*5)+(1*0)=186
186 % 10 = 6
So 98279-50-6 is a valid CAS Registry Number.
98279-50-6Relevant academic research and scientific papers
The Role of 2-α-Hydroxy- and 2-α-Oxo-2,3-cycloalkenopyridinium Intermediates During Decker Oxidation of Hydrogenated Cycloalkapyridinium Salts
Weber, Horst,Lippe, Gotelind von der
, p. 4086 - 4098 (2007/10/02)
In alkaline solution pyridinium salts 3 readily undergo hydrolysis to betains 4 which are oxidized by hexacyanoferrate(III) to a mixture of isomeric carboxylic acids 5 and 6 in excellent yields.Decker oxidation of compounds 2 results in the pyridones 11 as main products.Formation of 5 and 6 via intermediates 3 and 4 is realized only in case of the lower homologues 2 (n = 2,3) and has no quantitative significance.Predominantly oxidative cleavage of the carbocycle in 2 occurs directly with simultaneous formation of the 2-pyridone structure and elimination of 2-α-C asan aldehyde function.Resulting stable reaction products are α-hydroxycarboxylic acids 12 and acids 5 with a shortened aliphatic side chain.It is demonstrated that 2 and 3 are not necessarily formed as intermediates during the conversion of 1 into 5 by means of Decker oxidation.
