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CAS 401815-98-3

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2-Fluoropyridine-4-boronic acid

Description:
2-Fluoropyridine-4-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that also contains a fluorine substituent. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group. The presence of the fluorine atom in the pyridine ring can influence its reactivity and electronic properties, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The boronic acid functionality allows for participation in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, this compound may exhibit unique properties such as pH sensitivity and the ability to form complexes with diols, which can be exploited in various applications, including sensor technology and drug delivery systems. As with many boronic acids, it is important to handle this compound with care, as it may have specific safety and environmental considerations.
Formula:C5H5BFNO2
InChI:InChI=1/C5H5BFNO2/c7-5-3-4(6(9)10)1-2-8-5/h1-3,9-10H
SMILES:c1cnc(cc1B(O)O)F
Synonyms:
  • (2-Fluoropyridin-4-yl)boronic acid
  • Boronic acid, B-(2-fluoro-4-pyridinyl)-
  • 2-Fluoropyridine-Boronic Acid
  • 2-Fluoropyridin-4-Ylboronic Acid
  • 2-Fluoro-4-pyridinylboronic acid
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