317383-70-3 Usage
Uses
Used in Pharmaceutical Industry:
1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-3-oxo-, methyl ester (9CI) is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical structure and properties. Its antioxidant and anti-inflammatory characteristics contribute to the development of new medicinal products that can potentially treat a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-3-oxo-, methyl ester (9CI) is utilized as a key component in the synthesis of various agrochemicals. Its properties make it suitable for the development of products that can enhance crop protection and improve agricultural yields.
Used in Organic Chemistry:
1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-3-oxo-, methyl ester (9CI) is employed as a valuable intermediate in organic chemistry. Its unique structure allows for further functionalization and modification, leading to the creation of novel compounds with specific applications in various fields.
Used in Material Science:
1(2H)-Pyridinecarboxylicacid,3,6-dihydro-3-oxo-,methylester(9CI) also has potential applications in the field of material science. Its properties can be harnessed to develop new materials with improved characteristics, such as enhanced stability, reactivity, or selectivity, which can be beneficial in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 317383-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,8 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 317383-70:
(8*3)+(7*1)+(6*7)+(5*3)+(4*8)+(3*3)+(2*7)+(1*0)=143
143 % 10 = 3
So 317383-70-3 is a valid CAS Registry Number.
317383-70-3Relevant academic research and scientific papers
Malinakova,Liebeskind
, p. 3909 - 3911 (2000)
[reaction: see text] A chiral, nonracemic eta(3)-pyridinyl scaffold participates in [5 + 2] cycloaddition with electron-deficient alkenes, an allene, and an alkyne to give eta(3)-allylmolybdenum bicyclic adducts. The adducts can be demetalated, providing a convergent route to highly functionalized tropanes. High enantiocontrol can be achieved throughout the cycloaddition and demetalation sequence.
