3,5-Difluoro-4-morpholinophenylboronic Acid Pinacol Ester
95%
- Product Code: 89928
CAS:
1313738-69-0
| Molecular Weight: | 325.16 g./mol | Molecular Formula: | C₁₆H₂₂F₂NO₃B |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18375252 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, enabling the formation of carbon-carbon bonds. Its application is significant in the pharmaceutical industry, where it aids in the development of drug candidates by facilitating the incorporation of aryl groups into target structures. Additionally, it is employed in materials science for the synthesis of advanced organic materials, including polymers and liquid crystals, due to its stability and reactivity under mild conditions. Its role in catalysis and functional group transformations further extends its utility in research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿22,572.00 |
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3,5-Difluoro-4-morpholinophenylboronic Acid Pinacol Ester
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, enabling the formation of carbon-carbon bonds. Its application is significant in the pharmaceutical industry, where it aids in the development of drug candidates by facilitating the incorporation of aryl groups into target structures. Additionally, it is employed in materials science for the synthesis of advanced organic materials, including polymers and liquid crystals, due to its stability and reactivity under mild conditions. Its role in catalysis and functional group transformations further extends its utility in research and industrial processes.
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