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CAS 929250-35-1

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6-Benzyloxypyridine-3-boronic acid

Description:
6-Benzyloxypyridine-3-boronic acid is an organoboron compound characterized by the presence of a pyridine ring substituted with a benzyloxy group and a boronic acid functional group. The molecular structure features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, contributing to its basicity and potential for coordination with metal ions. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The benzyloxy group enhances the compound's lipophilicity, potentially improving its bioavailability. This compound is often utilized in cross-coupling reactions, particularly in the Suzuki-Miyaura reaction, which is a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its unique structural features may impart specific biological activities, making it a candidate for further research in drug development and material science. Overall, 6-Benzyloxypyridine-3-boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C12H12BNO3
InChI:InChI=1/C12H12BNO3/c15-13(16)11-6-7-12(14-8-11)17-9-10-4-2-1-3-5-10/h1-8,15-16H,9H2
InChI key:CUZOGAUUSKBDAO-UHFFFAOYSA-N
SMILES:c1ccc(cc1)COc1ccc(cn1)B(O)O
Synonyms:
  • [6-(Benzyloxy)pyridin-3-yl]boronic acid
  • Boronic acid, B-[6-(phenylmethoxy)-3-pyridinyl]-
  • 6-Benzyloxypyridin-3-ylboronic acid
  • 6-Benzyloxypyridine-3-boronicaci
  • 6-Benzyloxypyridine-3-boronic Acid (contains varying amounts of Anhydride)
  • 6-(benzyloxy)pyridin-3-yl-3-boronic acid
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