3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
97%
- Product Code: 194537
CAS:
844501-71-9
| Molecular Weight: | 194.041 g./mol | Molecular Formula: | C₉H₁₅BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07368044 | |
| Melting Point: | 105-108 °C | Boiling Point: | 335.4±15.0 °C(Predicted) |
| Density: | 1.09±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-nitrogen and carbon-carbon bonds under mild conditions. It is especially valuable in constructing pyrazole-based heterocyclic systems, which are common motifs in bioactive molecules. Due to its stability and reactivity, it is widely employed in medicinal chemistry for the development of kinase inhibitors, anti-inflammatory agents, and antiviral drugs. Additionally, it finds use in materials science for creating functional organic molecules with optoelectronic properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25g | 10-20 days | ฿3,460.00 |
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| 100g | 10-20 days | ฿12,730.00 |
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| 5g | 10-20 days | ฿700.00 |
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-nitrogen and carbon-carbon bonds under mild conditions. It is especially valuable in constructing pyrazole-based heterocyclic systems, which are common motifs in bioactive molecules. Due to its stability and reactivity, it is widely employed in medicinal chemistry for the development of kinase inhibitors, anti-inflammatory agents, and antiviral drugs. Additionally, it finds use in materials science for creating functional organic molecules with optoelectronic properties.
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