5-(1-Hydroxy-1-methylethyl-d6)-furan-2-boronic acid pinacol ester

95%

Reagent Code: #90754
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CAS Number 2223033-32-5

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Weight 276.166690668 g/mol
Formula C₁₃H₁₇BD₆O₅
inventory_2 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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Size Availability Unit Price Quantity
inventory 5mg
10-20 days €580.84
inventory 25mg
10-20 days €1,733.56
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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