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CAS 848243-23-2

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2-Ethoxypyridine-3-boronic acid pinacol ester

Description:
2-Ethoxypyridine-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyridine ring substituted with an ethoxy group and a boronic acid moiety that is esterified with pinacol. This compound typically exhibits properties associated with both boronic acids and pyridine derivatives, including moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in synthetic organic chemistry. The boronic acid functionality allows for the formation of covalent bonds with diols and can participate in Suzuki-Miyaura coupling reactions, which are essential for constructing carbon-carbon bonds. The presence of the ethoxy group enhances its solubility and may influence its reactivity. Additionally, the pinacol ester form stabilizes the boronic acid, making it easier to handle and store. Overall, this compound is of interest in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating functionalized polymers and other advanced materials.
Formula:C13H20BNO3
InChI:InChI=1/C13H20BNO3/c1-6-16-11-10(8-7-9-15-11)14-17-12(2,3)13(4,5)18-14/h7-9H,6H2,1-5H3
SMILES:CCOc1c(cccn1)B1OC(C)(C)C(C)(C)O1
Synonyms:
  • Pyridine, 2-Ethoxy-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-
  • 2-Ethoxy-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
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