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CAS 1171891-07-8

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5-Phenyl-3-pyridinyl boronic acid, pinacol ester

Description:
5-Phenyl-3-pyridinyl boronic acid, pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group that is esterified with pinacol. This compound features a pyridine ring and a phenyl group, contributing to its aromatic character and potential reactivity. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols and is widely utilized in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The pinacol ester form enhances its stability and solubility, facilitating its use in various chemical applications. Additionally, the compound may exhibit properties such as moderate polarity and potential biological activity, depending on the context of its use. Its structural features suggest potential applications in medicinal chemistry, materials science, and as a building block in the synthesis of more complex organic molecules. As with many organoboron compounds, careful handling and storage are recommended due to their sensitivity to moisture and air.
Formula:C17H20BNO2
InChI:InChI=1S/C17H20BNO2/c1-16(2)17(3,4)21-18(20-16)15-10-14(11-19-12-15)13-8-6-5-7-9-13/h5-12H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cc(cnc2)c2ccccc2)O1
Synonyms:
  • 3-Phenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • (5-Phenylpyridin-3-yl)boronic acid, pinacol ester
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