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CAS 850991-69-4

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5-Methoxypyridine-3-boronic acid

Description:
5-Methoxypyridine-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that also contains a methoxy substituent. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid group, which can engage in hydrogen bonding. The methoxy group enhances its solubility and may influence its reactivity. 5-Methoxypyridine-3-boronic acid is often utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for the formation of carbon-carbon bonds. Its boronic acid functionality allows it to form reversible complexes with diols, making it useful in various applications, including drug development and materials science. Additionally, the compound's stability and reactivity can be influenced by factors such as pH and the presence of other functional groups in a reaction mixture.
Formula:C6H8BNO3
InChI:InChI=1/C6H8BNO3/c1-11-6-2-5(7(9)10)3-8-4-6/h2-4,9-10H,1H3
SMILES:COc1cc(cnc1)B(O)O
Synonyms:
  • (5-Methoxypyridin-3-yl)boronic acid
  • boronic acid, B-(5-methoxy-3-pyridinyl)-
  • (5-Methoxy-3-Pyridinyl)Boronic Acid
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