2-(1-Boc-3,5-dimethyl-4-pyrazolyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
- Product Code: 89485
CAS:
1073354-70-7
| Molecular Weight: | 322.21 g./mol | Molecular Formula: | C₁₆H₂₇BN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09027070 | |
| Melting Point: | 112°C | 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 the Suzuki-Miyaura reaction. It serves as a valuable boronic ester reagent, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. Its Boc-protected pyrazole moiety enhances stability and selectivity during reactions, making it suitable for use in pharmaceutical research and the development of biologically active compounds. Additionally, it is employed in the synthesis of advanced materials and agrochemicals, where precise molecular assembly is critical. Its compatibility with various functional groups and reaction conditions makes it a versatile tool in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,484.00 |
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2-(1-Boc-3,5-dimethyl-4-pyrazolyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a valuable boronic ester reagent, enabling the formation of carbon-carbon bonds in the construction of complex organic molecules. Its Boc-protected pyrazole moiety enhances stability and selectivity during reactions, making it suitable for use in pharmaceutical research and the development of biologically active compounds. Additionally, it is employed in the synthesis of advanced materials and agrochemicals, where precise molecular assembly is critical. Its compatibility with various functional groups and reaction conditions makes it a versatile tool in modern synthetic chemistry.
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