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CAS 1171891-42-1

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5-methylpyridin-3-ylboronic acid pinacol ester

Description:
5-Methylpyridin-3-ylboronic acid pinacol ester is an organoboron compound characterized by the presence of a pyridine ring substituted with a methyl group and a boronic acid moiety that is esterified with pinacol. This compound typically exhibits properties associated with both boronic acids and pyridine derivatives, such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The boronic acid functionality allows for the formation of reversible covalent bonds with diols, which can be exploited in various applications, including drug development and materials science. Additionally, the presence of the methyl group on the pyridine ring can influence the electronic properties and steric hindrance, affecting its reactivity and interactions with other molecules. Overall, this compound serves as a useful building block in the synthesis of more complex organic molecules, particularly in the context of Suzuki-Miyaura coupling reactions.
Formula:C12H18BNO2
InChI:InChI=1S/C12H18BNO2/c1-9-6-10(8-14-7-9)13-15-11(2,3)12(4,5)16-13/h6-8H,1-5H3
InChI key:InChIKey=SYEVQHAWWSEMRN-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(C)C=NC2
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