CAS 1334607-79-2

4-Isopropanoxy-3-(trifluoromethyl)phenylboronic acid pinacol ester

Description:

4-Isopropanoxy-3-(trifluoromethyl)phenylboronic acid pinacol ester is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that features both an isopropanoxy group and a trifluoromethyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. Additionally, the pinacol ester moiety contributes to the stability of the boronic acid, allowing for easier handling and storage. Overall, this compound is of interest in medicinal chemistry and materials science due to its unique structural features and potential applications in drug development and catalysis. As with many boronic compounds, it may also exhibit specific solubility characteristics and reactivity patterns that are important for its use in synthetic pathways.

Formula: C₁₆H₂₂BF₃O₃

Synonyms:

• 4-Isopropanoxy-3-(trifluoromethyl)phenylboronic acid pinacol ester
• Pinacol 4-Isopropanoxy-3-(trifluoromethyl)benzeneboronate
• 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[4-(1-methylethoxy)-3-(trifluoromethyl)phenyl]-
• 4,4,5,5-Tetramethyl-2-[4-(1-methylethoxy)-3-(trifluoromethyl)phenyl]-1,3,2-dioxaborolane