259675-84-8 Usage
Uses
Used in Pharmaceutical Industry:
2-Amino-3,5,6-trifluoro-4-pyridinecarboxylic acid ethyl ester is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical structure and biological activities, including its antiviral, antibacterial, and antifungal properties. It contributes to the development of new drugs and treatments for a range of diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Amino-3,5,6-trifluoro-4-pyridinecarboxylic acid ethyl ester is utilized as a key component in the creation of pesticides and other agrochemical products, leveraging its biological activities to protect crops and enhance agricultural productivity.
Used in Chemical Research:
2-Amino-3,5,6-trifluoro-4-pyridinecarboxylic acid ethyl ester serves as a reagent in chemical research, facilitating various experimental procedures and the exploration of new chemical reactions and mechanisms.
Used as a Precursor in Organic Synthesis:
2-Amino-3,5,6-trifluoro-4-pyridinecarboxylicacidethylester is used as a precursor in the synthesis of other organic compounds, enabling the creation of a wide array of chemical entities for different applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 259675-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,6,7 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 259675-84:
(8*2)+(7*5)+(6*9)+(5*6)+(4*7)+(3*5)+(2*8)+(1*4)=198
198 % 10 = 8
So 259675-84-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7F3N2O2/c1-2-15-8(14)3-4(9)6(11)13-7(12)5(3)10/h2H2,1H3,(H2,12,13)
259675-84-8Relevant academic research and scientific papers
Preparation and reactions of 2,3,4,6-tetrafluoropyridine and its derivatives
Coe, Paul L.,Rees, Anthony J.
, p. 45 - 60 (2007/10/03)
A reliable route to 2,3,4,6-tetrafluoropyridine has been established starting from the readily available 3,5-dichlorotrifluoropyridine by halogen exchange under controlled conditions to give 3-chlorotetrafluoropyridine and its subsequent hydrodechlorination using hydrogen over palladium on alumina at 250-270°C. The formation and reactions of the 3-lithio derivative have been studied with the aim of obtaining 3,4-disubstituted trifluoropyridines. Routes to such materials have been developed and their conversion to deazapurine derivatives as potential substrates for the generation of anti-sense nucleosides are reported.
