3-Chlorophenyl boronic acid serves as a versatile biochemical reagent primarily utilized in 1,4-conjugate addition reactions and Suzuki-Miyaura cross-coupling reactions. Its reactivity with ethenesulfonamides leads to the formation of arylethanesulfonamides, while it is also employed in synthesizing biarylketones and phthalides. Additionally, 3-chlorophenyl boronic acid has applications in the development of phosphodiesterase 4 (PDE4) inhibitors and is valuable for investigating cellular processes such as migration and wound healing studies.
3-Chlorophenyl boronic acid serves as a versatile biochemical reagent primarily utilized in 1,4-conjugate addition reactions and Suzuki-Miyaura cross-coupling reactions. Its reactivity with ethenesulfonamides leads to the formation of arylethanesulfonamides, while it is also employed in synthesizing biarylketones and phthalides. Additionally, 3-chlorophenyl boronic acid has applications in the development of phosphodiesterase 4 (PDE4) inhibitors and is valuable for investigating cellular processes such as migration and wound healing studies.
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