
CAS 1218791-13-9
:4-(Cbz-amino)-2-Fluorophenylboronic acid pinacol ester
Description:
4-(Cbz-amino)-2-Fluorophenylboronic acid pinacol ester is a boronic acid derivative characterized by the presence of a fluorophenyl group and a carbobenzyloxy (Cbz) amino group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The presence of the fluorine atom can influence the electronic properties and reactivity of the molecule, potentially enhancing its selectivity in chemical reactions. Additionally, the pinacol ester moiety contributes to the stability and solubility of the compound, facilitating its handling and use in laboratory settings. The Cbz group serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the amine's reactivity. Overall, this compound is valuable in medicinal chemistry and materials science for its unique reactivity and functionalization potential.
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Found 3 products.
4-(Benzyloxycarbonylamino)-2-fluorophenylboronic acid, pinacol ester
CAS:Formula:C20H23BFNO4Purity:97%Color and Shape:SolidMolecular weight:371.21034-(Cbz-Amino)-2-fluorophenylboronic acid, pinacol ester
CAS:4-(Cbz-Amino)-2-fluorophenylboronic acid, pinacol esterPurity:95%Molecular weight:371.21g/molBenzyl (3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
CAS:Formula:C20H23BFNO4Purity:97%Molecular weight:371.22


