796090-24-9 Usage
Uses
Used in Pharmaceutical Industry:
6-Chloro-3-(trifluoromethyl)pyridine-2-carboxylic acid serves as a crucial building block for the synthesis of various drug molecules and APIs. Its unique structural features contribute to the development of new medications aimed at treating a wide array of diseases and medical conditions.
Used in Organic Synthesis:
Beyond its pharmaceutical applications, 6-Chloro-3-(trifluoromethyl)pyridine-2-carboxylic acid also functions as a reagent in organic synthesis. It aids in the creation of complex organic compounds, facilitating advancements in chemical research and the discovery of novel chemical entities.
Used in Chemical Research:
In the realm of chemical research, 6-Chloro-3-(trifluoromethyl)pyridine-2-carboxylic acid is utilized to explore and understand the properties and reactions of pyridine derivatives. Its presence in experimental setups can provide insights into the behavior of similar compounds and contribute to the broader understanding of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 796090-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,0,9 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 796090-24:
(8*7)+(7*9)+(6*6)+(5*0)+(4*9)+(3*0)+(2*2)+(1*4)=199
199 % 10 = 9
So 796090-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClF3NO2/c8-4-2-1-3(7(9,10)11)5(12-4)6(13)14/h1-2H,(H,13,14)
796090-24-9Relevant academic research and scientific papers
Three chloro(trifluoromethyl)pyridines as model substrates for regioexhaustive functionalization
Cottet, Fabrice,Schlosser, Manfred
, p. 3793 - 3798 (2007/10/03)
As a further test of the concept of regioexhaustive functionalization, 2-chloro-6-(trifluoromethyl)pyridine, 2-chloro-5-(trifluoromethyl)pyridine and 3-chloro-4-(trifluoromethyl)-pyridine were each converted into the three possible carboxylic acids 2, 4, 6, 8, 10, 12, 16, 17 and 20. This was achieved by employing several, but not all of the organometallic "tool-box methods": transformation of a more basic organometallic species into a less basic isomer by transmetalation-equilibration, site discriminating deprotonation with lithium N,N-diisopropylamide or lithium 2,2,6,6- tetramethylpiperidide, regio-divergent iodine migration and steric screening of acidic positions by a bulky trialkylsilyl group. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
