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CAS 904326-91-6

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(6-fluoro-2-methyl-3-pyridyl)boronic acid

Description:
(6-Fluoro-2-methyl-3-pyridyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. The structure features a fluorine atom at the 6-position and a methyl group at the 2-position of the pyridine, contributing to its unique reactivity and properties. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The boronic acid group allows for the formation of stable complexes with diols, making it useful in various applications, including medicinal chemistry and materials science. Additionally, the presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity. As with many boronic acids, it is important to handle this compound with care, as it can be sensitive to moisture and air, which may affect its stability and reactivity. Overall, (6-fluoro-2-methyl-3-pyridyl)boronic acid is a versatile building block in synthetic organic chemistry.
Formula:C6H7BFNO2
InChI:InChI=1/C6H7BFNO2/c1-4-5(7(10)11)2-3-6(8)9-4/h2-3,10-11H,1H3
SMILES:Cc1c(ccc(F)n1)B(O)O
Synonyms:
  • (6-Fluoro-2-Methylpyridin-3-Yl)Boronic Acid
  • boronic acid, B-(6-fluoro-2-methyl-3-pyridinyl)-
  • 2-Fluoro-6-methylpyridine-5-boronicacid
  • 2-Fluoro-6-methylpyridine-5-boronic acid
  • 6-Fluoro-2-methylpyridine-3-boronic acid
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