
CAS 1366482-32-7
:5-chloro-6-fluoropyridin-3-ylboronic acid
Description:
5-Chloro-6-fluoropyridin-3-ylboronic 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 a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the chlorine and fluorine substituents can influence its reactivity and polarity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in the synthesis of biaryl compounds. The boronic acid group allows for the formation of stable complexes with diols, which is significant in applications such as drug development and materials science. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as boronic acids can be sensitive to moisture and may require specific storage conditions.
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Found 3 products.
Boronic acid, B-(5-chloro-6-fluoro-3-pyridinyl)-
CAS:Formula:C5H4BClFNO2Purity:98%Color and Shape:SolidMolecular weight:175.3532(5-Chloro-6-fluoropyridin-3-yl)boronic acid
CAS:(5-Chloro-6-fluoropyridin-3-yl)boronic acidPurity:98%Molecular weight:175.35g/mol5-CHLORO-6-FLUOROPYRIDIN-3-YLBORONIC ACID
CAS:Formula:C5H4BClFNO2Purity:98%Color and Shape:SolidMolecular weight:175.35


