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CAS 854373-97-0

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2-Ethoxypyridine-3-boronic acid

Description:
2-Ethoxypyridine-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. 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 ethoxy group enhances its solubility and reactivity. It is often utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a boron source for the formation of carbon-carbon bonds. The compound's reactivity is influenced by the electron-withdrawing nature of the pyridine ring, which can stabilize the boronate intermediate formed during reactions. Additionally, 2-ethoxypyridine-3-boronic acid may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as with all boronic acids, due to potential irritant properties.
Formula:C7H10BNO3
InChI:InChI=1/C7H10BNO3/c1-2-12-7-6(8(10)11)4-3-5-9-7/h3-5,10-11H,2H2,1H3
SMILES:CCOc1c(cccn1)B(O)O
Synonyms:
  • (2-Ethoxypyridin-3-yl)boronic acid
  • boronic acid, B-(2-ethoxy-3-pyridinyl)-
  • 2-Ethoxy-3-pyridineboronicacid
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