(2-Methyl-5-pyrrolidino-d11)-thiophene-3-boronic acid pinacol ester
95%
- Product Code: 89030
CAS:
2223033-67-6
| Molecular Weight: | 322.315619558 g./mol | Molecular Formula: | C₁₅H₁₅BD₁₁NO₃S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿269,660.00 |
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| 0.025 | 10-20 days | ฿699,980.00 |
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(2-Methyl-5-pyrrolidino-d11)-thiophene-3-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 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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