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CAS 2121513-14-0

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B-(5-Ethoxy-6-fluoro-3-pyridinyl)boronic acid

Description:
B-(5-Ethoxy-6-fluoro-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The ethoxy group enhances its lipophilicity, potentially improving its bioavailability in pharmaceutical applications. The fluorine atom in the pyridine ring can influence the electronic properties of the molecule, often enhancing its reactivity and stability. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various chemical reactions, including Suzuki coupling, which is widely used in organic synthesis. Additionally, compounds like this one may exhibit biological activity, making them of interest in medicinal chemistry, particularly in the development of targeted therapies. Overall, B-(5-Ethoxy-6-fluoro-3-pyridinyl)boronic acid represents a versatile structure with potential applications in both synthetic and medicinal chemistry.
Formula:C7H9BFNO3
InChI:InChI=1S/C7H9BFNO3/c1-2-13-6-3-5(8(11)12)4-10-7(6)9/h3-4,11-12H,2H2,1H3
InChI key:InChIKey=DYZJVTGMDRHEJB-UHFFFAOYSA-N
SMILES:O(CC)C=1C=C(B(O)O)C=NC1F
Synonyms:
  • B-(5-Ethoxy-6-fluoro-3-pyridinyl)boronic acid
  • Boronic acid, B-(5-ethoxy-6-fluoro-3-pyridinyl)-
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