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CAS 500707-34-6

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(3-methoxypyridin-2-yl)boronic acid

Description:
(3-Methoxypyridin-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has a methoxy substituent. This compound typically appears as a white to off-white solid 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 the compound's solubility and can influence its reactivity. (3-Methoxypyridin-2-yl)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. Additionally, its boronic acid functionality allows it to form reversible complexes with diols, making it useful in various applications, including drug development and materials science. The compound's reactivity and functional versatility make it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals.
Formula:C6H8BNO3
InChI:InChI=1/C6H8BNO3/c1-11-5-3-2-4-8-6(5)7(9)10/h2-4,9-10H,1H3
Synonyms:
  • (3-Methoxypyridin-2-yl)boronic acid
  • boronic acid, B-(3-methoxy-2-pyridinyl)-
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