1-(2,2-Dimethoxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
≥98%
- Product Code: 179203
CAS:
864754-40-5
| Molecular Weight: | 282.14 g./mol | Molecular Formula: | C₁₃H₂₃BN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08706099 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Drying, Inert Gas |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. The presence of the pyrazole ring allows for the construction of nitrogen-containing heterocycles, which are common structural motifs in bioactive compounds. It is especially useful in medicinal chemistry for developing drug candidates and functional materials where precise molecular architecture is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿4,240.00 |
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| 1g | 10-20 days | ฿12,000.00 |
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| 5g | 10-20 days | ฿55,990.00 |
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1-(2,2-Dimethoxyethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. The presence of the pyrazole ring allows for the construction of nitrogen-containing heterocycles, which are common structural motifs in bioactive compounds. It is especially useful in medicinal chemistry for developing drug candidates and functional materials where precise molecular architecture is required.
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