CAS 1332334-01-6
:3-Fluoro-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester
Description:
3-Fluoro-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is further substituted with a fluorine atom and a pyrazole moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols and other Lewis bases, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The presence of the fluorine atom can enhance the compound's reactivity and influence its electronic properties, while the pyrazole ring may contribute to its biological activity. As a pinacol ester, it is generally more stable and less reactive than its corresponding boronic acid, facilitating easier handling and storage. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and the synthesis of complex organic molecules. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any risks associated with its use.
Formula:C15H18BFN2O2
Synonyms:- 3-Fluoro-4-(1H-pyrazol-1-yl)phenylboronic acid pinacol ester
- 1H-Pyrazole, 1-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
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Found 1 products.
1-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-pyrazole
CAS:1-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-pyrazolePurity:95%Molecular weight:288.13g/mol
