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CAS 196083-20-2

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[6-(2,2,2-Trifluoroethoxy)Pyridin-3-Yl]Boronic Acid

Description:
[6-(2,2,2-Trifluoroethoxy)Pyridin-3-Yl]Boronic Acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a trifluoroethoxy substituent at the 6-position of the pyridine, which enhances its lipophilicity and may influence its reactivity and solubility in organic solvents. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis, medicinal chemistry, and materials science. The trifluoroethoxy group can also impart unique electronic properties, potentially affecting the compound's reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, the presence of fluorine atoms often enhances the compound's stability and can influence its biological activity. Overall, [6-(2,2,2-Trifluoroethoxy)Pyridin-3-Yl]Boronic Acid is a versatile compound with potential applications in drug development and synthetic chemistry.
Formula:C7H7BF3NO3
InChI:InChI=1S/C7H7BF3NO3/c9-7(10,11)4-15-6-2-1-5(3-12-6)8(13)14/h1-3,13-14H,4H2
SMILES:c1cc(ncc1B(O)O)OCC(F)(F)F
Synonyms:
  • [6-(2,2,2-Trifluoroethoxy)-3-pyridinyl]boronic acid
  • 6-(2,2,2-trifluoroethoxy)pyridin-3-yl-3-boronic acid
  • [6-(2,2,2-TRIFLUOROETHOXY)PYRIDIN-3-YL]BORONIC ACID
  • Boronic acid, B-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]-
  • RB2068
  • [6-(2,2,2-trifluoroethoxy)-3-pyridyl]boronic acid
  • 6-(2,2,2-Trifluoroethoxy)pyridine-3-boronic acid
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