247564-72-3 Usage
Description
2,4,5-Trifluorophenylboronic acid is a synthetic compound characterized by its white to light yellow crystalline powder form. It is known for its unique chemical properties, which make it a valuable component in various chemical reactions and applications.
Uses
Used in Pharmaceutical Industry:
2,4,5-Trifluorophenylboronic acid is used as a synthetic intermediate for the development of pharmaceutical compounds. Its unique chemical structure allows it to be incorporated into the design of new drugs, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
In the field of chemical research, 2,4,5-Trifluorophenylboronic acid serves as a valuable reagent for conducting various chemical reactions. Its properties enable researchers to explore new reaction pathways and synthesize complex organic molecules.
Used in Material Science:
2,4,5-Trifluorophenylboronic acid is utilized in the development of advanced materials, such as polymers and coatings. Its unique chemical properties contribute to the creation of materials with improved properties, such as enhanced stability, durability, and performance.
Overall, 2,4,5-Trifluorophenylboronic acid is a versatile synthetic compound with a wide range of applications across different industries, including pharmaceuticals, chemical research, and material science. Its unique properties make it an essential component in the development of new technologies and products.
Check Digit Verification of cas no
The CAS Registry Mumber 247564-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,5,6 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 247564-72:
(8*2)+(7*4)+(6*7)+(5*5)+(4*6)+(3*4)+(2*7)+(1*2)=163
163 % 10 = 3
So 247564-72-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BF3O2/c8-4-2-6(10)5(9)1-3(4)7(11)12/h1-2,11-12H
247564-72-3Relevant articles and documents
Synthesis of Polyflourinated Biphenyls; Pushing the Boundaries of Suzuki-Miyaura Cross Coupling with Electron-Poor Substrates
Bulfield, David,Huber, Stefan M.
, p. 13188 - 13203 (2017/12/26)
Polyfluorinated biphenyls are interesting and promising substrates for many different applications. Unfortunately, all current methods for the syntheses of these compounds only work for a hand full of molecules or only in very special cases. Thus, many of these compounds are still inaccessible to date. Here we report a general strategy for the synthesis of a wide range of highly fluorinated biphenyls. In our studies we investigated crucial parameters, such as different phosphine ligands and the influence of various nucleophiles and electrophiles with different degrees of fluorination. These results extend the scope of the already very versatile Suzuki-Miyaura reaction toward the synthesis of very electron-poor products, making these more readily accessible. The presented methodology is scalable and versatile without the need for elaborate phosphine ligands or Pd-precatalysts.
