CAS 863868-36-4
:3,5-Difluorophenylboronic acidpinacol ester
Description:
3,5-Difluorophenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group esterified with pinacol. This compound features a phenyl ring substituted with two fluorine atoms at the 3 and 5 positions, which can influence its reactivity and solubility. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The pinacol ester form enhances stability and solubility compared to the free boronic acid. Typically, compounds like this are utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. The presence of fluorine atoms can also impart unique electronic properties, potentially affecting the compound's reactivity and interaction with biological targets. Overall, 3,5-Difluorophenylboronic acid pinacol ester is a valuable intermediate in the synthesis of complex organic molecules and pharmaceuticals.
Formula:C12H15BF2O2
Synonyms:- 3,5-Difluorophenylboronic acid, pinacol ester
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Found 4 products.
2-(3,5-Difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C12H15BF2O2Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:240.062-(3,5-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C12H15BF2O2Purity:98%Color and Shape:SolidMolecular weight:240.05413,5-Difluorophenylboronic acid, pinacol ester
CAS:3,5-Difluorophenylboronic acid, pinacol esterPurity:98%Color and Shape:SolidMolecular weight:240.05g/mol2-(3,5-Difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C12H15BF2O2Purity:95%Color and Shape:SolidMolecular weight:240.06



