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CAS 1256355-49-3

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B-[2-(4-Pyridinylmethoxy)phenyl]boronic acid

Description:
B-[2-(4-Pyridinylmethoxy)phenyl]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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a pyridinylmethoxy group, which enhances its solubility and reactivity. This structure allows for potential interactions with biological targets, making it of interest in drug discovery and development. The boronic acid moiety can participate in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the compound may exhibit properties such as moderate stability under ambient conditions, and its solubility can vary depending on the solvent used. Overall, B-[2-(4-Pyridinylmethoxy)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C12H12BNO3
InChI:InChI=1S/C12H12BNO3/c15-13(16)11-3-1-2-4-12(11)17-9-10-5-7-14-8-6-10/h1-8,15-16H,9H2
InChI key:InChIKey=KMRAOKJLIHHQJB-UHFFFAOYSA-N
SMILES:O(CC=1C=CN=CC1)C2=C(B(O)O)C=CC=C2
Synonyms:
  • Boronic acid, B-[2-(4-pyridinylmethoxy)phenyl]-
  • B-[2-(4-Pyridinylmethoxy)phenyl]boronic acid
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