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CAS 163105-90-6

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2-Methoxypyridine-3-boronic acid

Description:
2-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. It is known for its utility in organic synthesis, particularly in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds. The methoxy group enhances the electronic properties of the pyridine ring, influencing its reactivity and interaction with other reagents. Additionally, the boronic acid moiety can form reversible complexes with diols, making it useful in various applications, including sensor technology and drug development. Safety data should be consulted, as boronic acids can be sensitive to moisture and may require careful handling.
Formula:C6H8BNO3
InChI:InChI=1/C6H8BNO3/c1-11-6-5(7(9)10)3-2-4-8-6/h2-4,9-10H,1H3
SMILES:COc1c(cccn1)B(O)O
Synonyms:
  • 2-Methoxy-3-Pyridinyl Boronic Acid
  • 2-Methoxy-3-Pyridyl Boronic Acid
  • 2-Methoxy-3-Pyridineboronic Acid
  • 2-Methoxypyridin-3-Ylboronic Acid
  • 2-Methoxypyridin-3-Ylboronic Acid Hydrate
  • 2-Methoxypyridine-3-Boronic Acid Hydrate
  • 2-Methoxypyridyl-3-Boronic Acid Hydrate
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