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CAS 904326-92-7

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(6-Fluoro-5-methylpyridin-3-yl)boronic acid

Description:
(6-Fluoro-5-methylpyridin-3-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. The molecular structure features a pyridine ring substituted at the 3-position with a boronic acid group and at the 6-position with a fluorine atom, along with a methyl group at the 5-position. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. It is often utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds. The presence of the fluorine atom can enhance the compound's reactivity and influence its electronic properties, making it valuable in medicinal chemistry and material science. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including drug delivery and sensor development.
Formula:C6H7BFNO2
InChI:InChI=1S/C6H7BFNO2/c1-4-2-5(7(10)11)3-9-6(4)8/h2-3,10-11H,1H3
InChI key:InChIKey=XCWIMBMPJGQNHG-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(C)C(F)=NC1
Synonyms:
  • (2-Fluoro-3-methylpyridin-5-yl)boronic acid
  • 2-Fluoro-3-methylpyridine-5-boronic acid
  • 6-Fluoro-5-methylpyridine-3-boronic acid
  • 6-Fluoro-5-methylpyridine-3-boronicacid
  • B-(6-Fluoro-5-methyl-3-pyridinyl)boronic acid
  • Boronic acid, (6-fluoro-5-methyl-3-pyridinyl)-
  • Boronic acid, B-(6-fluoro-5-methyl-3-pyridinyl)-
  • (6-Fluoro-5-methylpyridin-3-yl)boronic acid
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