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CAS 1451392-17-8

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B-(2-Fluoro-5-methoxy-4-pyridinyl)boronic acid

Description:
B-(2-Fluoro-5-methoxy-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that is substituted with a fluorine atom and a methoxy group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity, while the methoxy group may affect its electronic properties and solubility. B-(2-Fluoro-5-methoxy-4-pyridinyl)boronic acid is often utilized in the development of pharmaceuticals and agrochemicals, as well as in cross-coupling reactions in organic synthesis. Its unique structural features contribute to its reactivity and potential applications in various chemical processes. As with many boronic acids, it is important to handle this compound with care due to its sensitivity to moisture and air.
Formula:C6H7BFNO3
InChI:InChI=1S/C6H7BFNO3/c1-12-5-3-9-6(8)2-4(5)7(10)11/h2-3,10-11H,1H3
InChI key:InChIKey=MFXOCJQHJRUNJF-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(OC)=CN=C(F)C1
Synonyms:
  • Boronic acid, B-(2-fluoro-5-methoxy-4-pyridinyl)-
  • B-(2-Fluoro-5-methoxy-4-pyridinyl)boronic acid
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