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CAS 955374-17-1

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B-[2-Fluoro-6-(4-morpholinyl)-3-pyridinyl]boronic acid

Description:
B-[2-Fluoro-6-(4-morpholinyl)-3-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a pyridine ring substituted with a fluorine atom and a morpholine moiety, contributing to its potential biological activity and solubility properties. The presence of the morpholine group may enhance its interaction with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The boronic acid functionality allows for participation in Suzuki coupling reactions, a valuable tool in organic synthesis for forming carbon-carbon bonds. Additionally, the compound's structure suggests potential applications in areas such as drug discovery and development, especially in targeting specific enzymes or receptors. Its unique characteristics, including its molecular geometry and electronic properties, can influence its reactivity and interactions in various chemical environments.
Formula:C9H12BFN2O3
InChI:InChI=1S/C9H12BFN2O3/c11-9-7(10(14)15)1-2-8(12-9)13-3-5-16-6-4-13/h1-2,14-15H,3-6H2
InChI key:InChIKey=PUIOCXIPPAMHSB-UHFFFAOYSA-N
SMILES:FC1=NC(=CC=C1B(O)O)N2CCOCC2
Synonyms:
  • Boronic acid, B-[2-fluoro-6-(4-morpholinyl)-3-pyridinyl]-
  • 2-Fluoro-6-morpholinopyridin-3-ylboronic acid
  • B-[2-Fluoro-6-(4-morpholinyl)-3-pyridinyl]boronic acid
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