3-Phenyl-1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
≥95%
- Product Code: 45676
CAS:
1028092-65-0
| Molecular Weight: | 354.25 g./mol | Molecular Formula: | C₂₀H₂₇BN₂O₃ |
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| EC Number: | MDL Number: | MFCD21602040 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a tetrahydro-2H-pyran (THP) protecting group and a boronate ester moiety, makes it valuable for constructing complex molecules, especially in pharmaceutical research. The THP group provides stability and selectivity during synthetic processes, while the boronate ester facilitates the formation of carbon-carbon bonds. It is often employed in the development of bioactive compounds, including drug candidates, due to its ability to introduce phenyl and pyrazole functionalities into target molecules. Additionally, its stability under various reaction conditions makes it a versatile reagent in medicinal chemistry and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,100.00 |
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| 0.250 | 10-20 days | ฿16,209.00 |
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3-Phenyl-1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a tetrahydro-2H-pyran (THP) protecting group and a boronate ester moiety, makes it valuable for constructing complex molecules, especially in pharmaceutical research. The THP group provides stability and selectivity during synthetic processes, while the boronate ester facilitates the formation of carbon-carbon bonds. It is often employed in the development of bioactive compounds, including drug candidates, due to its ability to introduce phenyl and pyrazole functionalities into target molecules. Additionally, its stability under various reaction conditions makes it a versatile reagent in medicinal chemistry and material science applications.
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