3,5-Dimethyl-1-(2-tetrahydropyranyl)-1H-pyrazole-4-boronic acid pinacol ester
97%
- Product Code: 89936
CAS:
1126779-11-0
| Molecular Weight: | 306.21 g./mol | Molecular Formula: | C₁₆H₂₇BN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12031452 | |
| Melting Point: | Boiling Point: | 435.3 °C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules. It is often employed in pharmaceutical research for the development of drug candidates, as well as in materials science for creating advanced polymers and functional materials. The tetrahydropyranyl group provides stability and protection during synthetic processes, enhancing its utility in multi-step reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,780.00 |
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| 1.000 | 10-20 days | ฿8,991.00 |
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3,5-Dimethyl-1-(2-tetrahydropyranyl)-1H-pyrazole-4-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules. It is often employed in pharmaceutical research for the development of drug candidates, as well as in materials science for creating advanced polymers and functional materials. The tetrahydropyranyl group provides stability and protection during synthetic processes, enhancing its utility in multi-step reactions.
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