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CAS 485799-04-0

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6-(4-Morpholinyl)pyridine-3-boronic acid pinacol ester

Description:
6-(4-Morpholinyl)pyridine-3-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is crucial for applications in medicinal chemistry and organic synthesis. The presence of the pyridine ring contributes to its aromatic properties, while the morpholine group enhances its solubility and potential biological activity. This compound typically exhibits moderate polarity due to the combination of the polar boronic acid moiety and the more hydrophobic aromatic and morpholine components. It is often utilized in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules. The pinacol ester group serves to protect the boronic acid during reactions, allowing for selective transformations. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 6-(4-Morpholinyl)pyridine-3-boronic acid pinacol ester is a versatile building block in organic synthesis with potential applications in drug discovery and development.
Formula:C15H23BN2O3
InChI:InChI=1/C15H23BN2O3/c1-14(2)15(3,4)21-16(20-14)12-5-6-13(17-11-12)18-7-9-19-10-8-18/h5-6,11H,7-10H2,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc(nc2)N2CCOCC2)O1
Synonyms:
  • 4-[5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-2-Pyridinyl]Morpholine
  • Morpholine, 4-[5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-2-Pyridinyl]-
  • 4-[5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridin-2-Yl]Morpholine
  • 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester
  • 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester
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