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CAS 1383625-22-6

:

2-Trifluoromethyl-pyridine-3-boronic acid pinacol ester

Description:
2-Trifluoromethyl-pyridine-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group esterified with pinacol, along with a trifluoromethyl-substituted pyridine ring. This compound typically exhibits properties associated with both boronic acids and pyridine derivatives, such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in synthetic organic chemistry. The trifluoromethyl group enhances the compound's lipophilicity and can influence its electronic properties, potentially affecting its reactivity and interactions in various chemical environments. Additionally, the pinacol ester moiety provides stability and can facilitate the handling and storage of the boronic acid functionality. This compound may be utilized in the development of pharmaceuticals, agrochemicals, or as a building block in complex organic synthesis, particularly in reactions involving Suzuki coupling or other boron-mediated transformations. Its unique structural features contribute to its utility in various chemical applications.
Formula:C12H15BF3NO2
Synonyms:
  • 2-Trifluoromethyl-pyridine-3-boronic acid picol ester
  • 2-Trifluoromethyl-pyridine-3-boronic acid pinacol ester
  • 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine
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