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CAS 951677-47-7

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B-(2-Chloro-5-fluoro-4-pyridinyl)boronic acid

Description:
B-(2-Chloro-5-fluoro-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 chlorine and fluorine atoms. This compound typically exhibits properties such as being a white to off-white solid, and it is soluble in polar solvents like water and alcohols, which is a common trait for boronic acids. The presence of the boronic acid group allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The chlorine and fluorine substituents on the pyridine ring can influence the compound's reactivity and biological activity, potentially enhancing its pharmacological properties. Additionally, due to its boron content, it may exhibit unique interactions with biological molecules, which can be leveraged in drug design and development. Overall, B-(2-Chloro-5-fluoro-4-pyridinyl)boronic acid is a versatile compound with applications in both synthetic and medicinal chemistry.
Formula:C5H4BClFNO2
InChI:InChI=1S/C5H4BClFNO2/c7-5-1-3(6(10)11)4(8)2-9-5/h1-2,10-11H
InChI key:InChIKey=JJHRCHRHBBOCGY-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C(F)=CN=C(Cl)C1
Synonyms:
  • (2-Chloro-5-fluoropyridin-4-yl)boronic acid
  • 2-Chloro-5-fluoropyridine-4-boronic acid
  • B-(2-Chloro-5-fluoro-4-pyridinyl)boronic acid
  • boronic acid, B-(2-chloro-5-fluoro-4-pyridinyl)-
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