1042986-00-4 Usage
Uses
Used in Medicinal Chemistry:
2-Fluoro-5-methylpyridine-3-carboxylic acid is used as a building block for the development of new pharmaceuticals due to its unique structure and properties that facilitate the synthesis of biologically active molecules.
Used in Organic Synthesis:
In the field of organic synthesis, 2-fluoro-5-methylpyridine-3-carboxylic acid is used as a reagent to create new compounds for further study and potential application in various industries, leveraging its structural characteristics to enhance compound development.
Used in Drug Development:
2-Fluoro-5-methylpyridine-3-carboxylic acid is employed as a precursor in drug development, contributing to the creation of potential new medications that can address unmet medical needs, thanks to its potential pharmacological activities.
Used in Agrochemicals:
2-fluoro-5-methylpyridine-3-carboxylic acid is also utilized in the agrochemical industry as a building block for the synthesis of biologically active molecules that can be used in the development of new pesticides or other agricultural chemicals, capitalizing on its unique structural features to improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 1042986-00-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,9,8 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1042986-00:
(9*1)+(8*0)+(7*4)+(6*2)+(5*9)+(4*8)+(3*6)+(2*0)+(1*0)=144
144 % 10 = 4
So 1042986-00-4 is a valid CAS Registry Number.
1042986-00-4Relevant academic research and scientific papers
Honeycutt, Aaron P.,Hoover, Jessica M.
, p. 7216 - 7219 (2018)
A nickel-catalyzed oxidative decarboxylative annulation reaction of simple benzamides and (hetero)aromatic carboxylates has been developed. This reaction provides access to a large array of phenanthridinones and their heterocyclic analogues, highlighting the utility and versatility of oxidative decarboxylative coupling strategies for C-C bond formation.
