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CAS 1072944-18-3

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2-Fluoro-4-methylpyridine-5-boronicacid

Description:
2-Fluoro-4-methylpyridine-5-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 fluorine atom at the 2-position and a methyl group at the 4-position of the pyridine, with the boronic acid group located at the 5-position. This compound is typically used in organic synthesis, particularly in Suzuki coupling reactions, which are valuable for forming carbon-carbon bonds. The presence of the boronic acid group allows for the formation of stable complexes with diols, making it useful in various applications, including drug development and material science. Additionally, the fluorine substituent can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and air, which can affect its stability and reactivity.
Formula:C6H7BFNO2
InChI:InChI=1S/C6H7BFNO2/c1-4-2-6(8)9-3-5(4)7(10)11/h2-3,10-11H,1H3
SMILES:Cc1cc(F)ncc1B(O)O
Synonyms:
  • 2-Fluoro-4-methylpyridine-5-boronic acid
  • 6-Fluoro-4-Methylpyridine-3-Boronic Acid
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