(2-Methyl-5-pyrrolidino-d11)-thiophene-3-boronic acid pinacol ester

95%

Reagent Code: #89030
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CAS Number 2223033-67-6

science Other reagents with same CAS 2223033-67-6

blur_circular Chemical Specifications

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Weight 322.315619558 g/mol
Formula C₁₅H₁₅BD₁₁NO₃S
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 functionality makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuterium labeling (d11) in the structure is particularly useful in mechanistic studies and isotopic labeling experiments, aiding in the tracking and analysis of chemical pathways. Its stability and reactivity make it a preferred choice in research and industrial applications where precise and efficient coupling reactions are required.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿269,660.00
inventory 25mg
10-20 days ฿699,980.00

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(2-Methyl-5-pyrrolidino-d11)-thiophene-3-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester functionality makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuterium labeling (d11) in the structure is particularly useful in mechanistic studies and isotopic labeling experiments, ai

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester functionality makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuterium labeling (d11) in the structure is particularly useful in mechanistic studies and isotopic labeling experiments, aiding in the tracking and analysis of chemical pathways. Its stability and reactivity make it a preferred choice in research and industrial applications where precise and efficient coupling reactions are required.

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