CAS 957065-87-1
:(2,6-difluoro-4-hydroxy-phenyl)boronic acid
Description:
(2,6-Difluoro-4-hydroxy-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenolic structure. This compound features two fluorine atoms substituted at the 2 and 6 positions of the phenyl ring, which can influence its electronic properties and reactivity. The hydroxyl group at the 4-position contributes to its acidity and potential for hydrogen bonding, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. The boronic acid moiety allows for the formation of stable complexes with diols, enhancing its utility in organic synthesis and materials science. Additionally, the presence of fluorine atoms can enhance lipophilicity and alter the compound's biological activity, making it of interest in medicinal chemistry. Overall, (2,6-difluoro-4-hydroxy-phenyl)boronic acid is a versatile compound with applications in organic synthesis, pharmaceuticals, and materials development.
Formula:C6H5BF2O3
InChI:InChI=1/C6H5BF2O3/c8-4-1-3(10)2-5(9)6(4)7(11)12/h1-2,10-12H
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Found 3 products.
2,6-difluoro-4-hydroxyphenylboronic acid
CAS:Formula:C6H5BF2O3Purity:96%Color and Shape:SolidMolecular weight:173.90992,6-Difluoro-4-hydroxybenzeneboronic acid
CAS:<p>2,6-Difluoro-4-hydroxybenzeneboronic acid</p>Formula:C6H5BF2O3Purity:95%Color and Shape: beige solidMolecular weight:173.91g/mol(2,6-Difluoro-4-hydroxyphenyl)boronic acid
CAS:Formula:C6H5BF2O3Purity:96%Color and Shape:Liquid, No data available.Molecular weight:173.91


