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CAS 906744-85-2

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2-Fluoro-6-methylpyridine-3-boronic acid

Description:
2-Fluoro-6-methylpyridine-3-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 at the 2-position and a methyl group at the 6-position of the pyridine, which influences its reactivity and solubility. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's electronic properties, potentially affecting its interactions in biological systems. Additionally, the methyl group can influence steric hindrance and the overall polarity of the molecule. This compound is typically used 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. Overall, 2-Fluoro-6-methylpyridine-3-boronic acid is a versatile building block in synthetic chemistry.
Formula:C6H7BFNO2
InChI:InChI=1/C6H7BFNO2/c1-4-2-3-5(7(10)11)6(8)9-4/h2-3,10-11H,1H3
SMILES:Cc1ccc(c(F)n1)B(O)O
Synonyms:
  • 2-Fluoro-6-picoline-3-boronic acid
  • (2-Fluoro-6-Methylpyridin-3-Yl)Boronic Acid
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