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CAS 1072952-44-3

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B-(3-Fluoro-5-methyl-4-pyridinyl)boronic acid

Description:
B-(3-Fluoro-5-methyl-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a fluorine atom and a methyl group at specific positions on the pyridine, which can influence its reactivity and solubility. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the fluorine atom can enhance the compound's biological activity and lipophilicity, while the methyl group may affect steric hindrance and electronic properties. B-(3-Fluoro-5-methyl-4-pyridinyl)boronic acid is often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structural features make it a subject of interest in various research fields, including drug discovery and materials science.
Formula:C6H7BFNO2
InChI:InChI=1S/C6H7BFNO2/c1-4-2-9-3-5(8)6(4)7(10)11/h2-3,10-11H,1H3
InChI key:InChIKey=PEGYCPMGAITWDN-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(C)=CN=CC1F
Synonyms:
  • B-(3-Fluoro-5-methyl-4-pyridinyl)boronic acid
  • 3-Fluoro-5-methylpyridine-4-boronic acid
  • Boronic acid, B-(3-fluoro-5-methyl-4-pyridinyl)-
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