5-(1-Hydroxy-1-methylethyl-d6)-furan-2-boronic acid pinacol ester
95%
Reagent
Code: #90754
CAS Number
2223033-32-5
blur_circular Chemical Specifications
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Molecular Information
Weight
276.166690668 g/mol
Formula
C₁₃H₁₇BD₆O₅
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Storage & Handling
Storage
-20°C, sealed, dry
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular structure is critical. The deuterated methyl groups in the compound can be useful in isotopic labeling studies, aiding in mechanistic investigations or tracking metabolic pathways in drug development. Its stability and reactivity make it a preferred choice in research and industrial applications requiring high selectivity and efficiency in chemical transformations.
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5-(1-Hydroxy-1-methylethyl-d6)-furan-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester functional group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular structure is critical. The deuterated methyl groups in the compound can be useful in isotopic labeling studies, aiding in mechanistic investigations or tracking metabolic pathways in drug development. Its stability and reactivity make it a preferred choice in research and industrial applications requiring high selectivity and efficiency in chemical transformations.
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