3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-trityl-1H-pyrazolo[3,4-b]pyridine
95%
- Product Code: 44321
CAS:
1319591-26-8
| Molecular Weight: | 487.3998 g./mol | Molecular Formula: | C₃₁H₃₀BN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26393423 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is widely employed in the pharmaceutical and material science industries. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds, which is crucial for constructing complex molecular structures. The trityl-protected pyrazolopyridine moiety enhances stability and selectivity during reactions, making it valuable for synthesizing biologically active compounds, including potential drug candidates. Its application extends to the development of advanced materials, where precise molecular architecture is required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿3,546.00 |
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-trityl-1H-pyrazolo[3,4-b]pyridine
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is widely employed in the pharmaceutical and material science industries. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds, which is crucial for constructing complex molecular structures. The trityl-protected pyrazolopyridine moiety enhances stability and selectivity during reactions, making it valuable for synthesizing biologically active compounds, including potential drug candidates. Its application extends to the development of advanced materials, where precise molecular architecture is required.
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