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CAS 1162257-58-0

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5-(Trifluoromethyl)pyridine-2-boronic acid

Description:
5-(Trifluoromethyl)pyridine-2-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has a trifluoromethyl substituent at the 5-position. This compound typically exhibits properties associated with both boronic acids and pyridine derivatives, including moderate solubility in polar solvents and potential reactivity in various chemical transformations, such as Suzuki coupling reactions. The trifluoromethyl group enhances the compound's lipophilicity and can influence its electronic properties, making it a valuable building block in medicinal chemistry and materials science. Additionally, the boronic acid functionality allows for the formation of reversible covalent bonds with diols, which is useful in drug design and sensor applications. The compound's stability, reactivity, and functionalization potential make it a subject of interest in synthetic organic chemistry. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken.
Formula:C6H5BF3NO2
InChI:InChI=1S/C6H5BF3NO2/c8-6(9,10)4-1-2-5(7(12)13)11-3-4/h1-3,12-13H
SMILES:c1cc(B(O)O)ncc1C(F)(F)F
Synonyms:
  • [5-(Trifluoromethyl)-2-pyridinyl]boronic acid
  • [5-(Trifluoromethyl)-2-pyridyl]boronic acid
  • 5-(Trifluoromethyl)Pyridin-2-Ylboronic Acid
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