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CAS 2121513-18-4

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B-(6-Fluoro-5-phenyl-3-pyridinyl)boronic acid

Description:
B-(6-Fluoro-5-phenyl-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 and other nucleophiles. This compound features a pyridine ring substituted with a fluorine atom and a phenyl group, contributing to its unique electronic and steric properties. The presence of the boronic acid moiety allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as boronic acids are often used in drug design and synthesis. Additionally, the fluorine substitution can enhance the compound's lipophilicity and metabolic stability. The compound's structure suggests it may participate in various chemical reactions, including Suzuki coupling, which is a widely used method for forming carbon-carbon bonds in organic synthesis. Overall, B-(6-Fluoro-5-phenyl-3-pyridinyl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C11H9BFNO2
InChI:InChI=1S/C11H9BFNO2/c13-11-10(8-4-2-1-3-5-8)6-9(7-14-11)12(15)16/h1-7,15-16H
InChI key:InChIKey=FVZACERYYLLMDU-UHFFFAOYSA-N
SMILES:FC1=C(C=C(B(O)O)C=N1)C2=CC=CC=C2
Synonyms:
  • B-(6-Fluoro-5-phenyl-3-pyridinyl)boronic acid
  • Boronic acid, B-(6-fluoro-5-phenyl-3-pyridinyl)-
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