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CAS 1034659-38-5

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(5-CHLORO-2-FLUOROPYRIDIN-4-YL)BORONIC ACID

Description:
(5-Chloro-2-fluoropyridin-4-yl)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 moderate solubility in polar solvents, which is common for boronic acids, and it may participate in various chemical reactions, including Suzuki coupling, due to the reactivity of the boronic acid moiety. The presence of halogen substituents (chlorine and fluorine) can influence the electronic properties of the molecule, potentially enhancing its reactivity and making it useful in medicinal chemistry and material science. Additionally, the compound may exhibit specific biological activities, making it of interest in pharmaceutical research. Its structural features allow for potential applications in the synthesis of complex organic molecules and in the development of agrochemicals or pharmaceuticals. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C5H4BClFNO2
Synonyms:
  • Boronic acid, B-(5-chloro-2-fluoro-4-pyridinyl)-
  • B-(5-Chloro-2-fluoro-4-pyridinyl)boronicacid
  • 5-Chloro-2-fluoropyridine-4-boronic acid
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90
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95
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100
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