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CAS 918138-38-2

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B-[6-(3-Pyridinyloxy)-3-pyridinyl]boronic acid

Description:
B-[6-(3-Pyridinyloxy)-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, making it useful in various chemical applications, including drug development and materials science. The compound features a pyridine ring substituted with a pyridinyloxy group, contributing to its potential biological activity and interaction with biological targets. Its boronic acid moiety allows for participation in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. The compound's solubility and stability can vary depending on the pH and the presence of other functional groups. Additionally, its unique structure may impart specific pharmacological properties, making it of interest in medicinal chemistry. Overall, B-[6-(3-Pyridinyloxy)-3-pyridinyl]boronic acid exemplifies the versatility of boronic acids in both synthetic and biological contexts.
Formula:C10H9BN2O3
InChI:InChI=1S/C10H9BN2O3/c14-11(15)8-3-4-10(13-6-8)16-9-2-1-5-12-7-9/h1-7,14-15H
InChI key:InChIKey=OKBZLPTXOVQGGP-UHFFFAOYSA-N
SMILES:O(C1=CC=C(B(O)O)C=N1)C=2C=CC=NC2
Synonyms:
  • B-[6-(3-Pyridinyloxy)-3-pyridinyl]boronic acid
  • [6-(Pyridin-3-yloxy)pyridin-3-yl]boronic acid
  • (6-(Pyridin-3-yloxy)pyridin-3-yl)boronicacid
  • Boronic acid, B-[6-(3-pyridinyloxy)-3-pyridinyl]-
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