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CAS 2121514-00-7

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B-(2-Fluoro-5-phenyl-3-pyridinyl)boronic acid

Description:
B-(2-Fluoro-5-phenyl-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that is further substituted with a fluorine atom and a phenyl group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can influence the compound's electronic properties and reactivity, while the phenyl group may enhance its lipophilicity and stability. B-(2-Fluoro-5-phenyl-3-pyridinyl)boronic acid may also participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the formation of carbon-carbon bonds. Its unique structure and functional groups suggest potential applications in drug development and materials science, particularly in the design of biologically active molecules or as intermediates in synthetic pathways. As with many boronic acids, care should be taken in handling due to their sensitivity to moisture and air.
Formula:C11H9BFNO2
InChI:InChI=1S/C11H9BFNO2/c13-11-10(12(15)16)6-9(7-14-11)8-4-2-1-3-5-8/h1-7,15-16H
InChI key:InChIKey=KJPJTWLGLBIZPD-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(=CN=C1F)C2=CC=CC=C2
Synonyms:
  • B-(2-Fluoro-5-phenyl-3-pyridinyl)boronic acid
  • Boronic acid, B-(2-fluoro-5-phenyl-3-pyridinyl)-
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