1479-96-5 Usage
Uses
Used in Pharmaceutical Industry:
5-Fluoropyridine-2,3-dicarboxylic acid is used as a key intermediate in the production of various drugs. Its unique structure and properties contribute to the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
5-Fluoropyridine-2,3-dicarboxylic acid is used as a key intermediate in the synthesis of agrochemicals. Its incorporation into these products can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used in Research and Development:
5-Fluoropyridine-2,3-dicarboxylic acid is utilized in research and development for the exploration of new chemical compounds and technologies. Its unique properties make it a valuable tool in advancing the field of organic chemistry and discovering novel applications.
Used in Material Development:
5-Fluoropyridine-2,3-dicarboxylic acid has potential applications in the development of new materials. Its unique structure and properties can be leveraged to create innovative materials with specific characteristics for various industries.
Overall, 5-fluoropyridine-2,3-dicarboxylic acid plays a crucial role in various industries and scientific endeavors, from pharmaceutical and agrochemical synthesis to research and material development. Its unique structure and properties make it a valuable compound for further exploration and application.
Check Digit Verification of cas no
The CAS Registry Mumber 1479-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1479-96:
(6*1)+(5*4)+(4*7)+(3*9)+(2*9)+(1*6)=105
105 % 10 = 5
So 1479-96-5 is a valid CAS Registry Number.
1479-96-5Relevant academic research and scientific papers
Oxidation of 2- and 3-Halogenated Quinolines: An Easy Access to 5- and 6-Halogenopyridine-2,3-dicarboxylic Acids
Bas, Marie-Delphine Le,Gueret, Caroline,Perrio, Cecile,Lasne, Marie-Claire,Barre, Louisa
, p. 2495 - 2499 (2007/10/03)
Pyridine-2,3-dicarboxylic acids bearing an halogen in the position α or β to the nitrogen atom were synthesized by oxidation of the corresponding quinolines. Two methods, using either ozone followed by hydrogen peroxide or ruthenium tetroxide under catalytic conditions were used. Diacids 1b,c and 2a-c substituted in 6-position by a chlorine or bromine and in 5-position by a fluorine, chlorine or bromine, respectively, were isolated in yields ranging from 46-71 percent. Yields of 6-fluoro and 6- or 5-iodo diacids 1a,d and 2d did not exceed 30 percent.
