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CAS 1070774-29-6

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B-(3-Fluoro-2-pyridinyl)boronic acid

Description:
B-(3-Fluoro-2-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has a fluorine substituent at the 3-position. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group, which can engage in hydrogen bonding. The presence of the fluorine atom can influence the electronic properties of the pyridine ring, potentially enhancing its reactivity in various chemical reactions, including Suzuki coupling reactions, which are widely used in organic synthesis for forming carbon-carbon bonds. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in the development of sensors and in medicinal chemistry for drug design. The compound's unique structure and reactivity profile make it valuable in both academic research and industrial applications, particularly in the synthesis of complex organic molecules.
Formula:C5H5BFNO2
InChI:InChI=1S/C5H5BFNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3,9-10H
InChI key:InChIKey=LTAUVGYDXJTVQB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=CC=N1
Synonyms:
  • 3-Fluoropyridine-2-boronic acid
  • Boronic acid, B-(3-fluoro-2-pyridinyl)-
  • (3-Fluoropyridin-2-yl)boronic acid
  • B-(3-Fluoro-2-pyridinyl)boronic acid
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