1-(4-Methoxybenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
≥95%
- Product Code: 210970
CAS:
1105039-88-0
| Molecular Weight: | 314.19 g./mol | Molecular Formula: | C₁₇H₂₃BN₂O₃ |
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| EC Number: | MDL Number: | MFCD16877287 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert gas storage |
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 reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 4-methoxybenzyl-substituted pyrazole moiety into target structures, which can enhance biological activity in drug discovery programs. Its stability and reactivity profile make it suitable for late-stage functionalization in multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,010.00 |
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| 250mg | 10-20 days | ฿1,250.00 |
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| 5g | 10-20 days | ฿17,600.00 |
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| 25g | 10-20 days | ฿85,040.00 |
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| 1g | 10-20 days | ฿4,240.00 |
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1-(4-Methoxybenzyl)-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 reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 4-methoxybenzyl-substituted pyrazole moiety into target structures, which can enhance biological activity in drug discovery programs. Its stability and reactivity profile make it suitable for late-stage functionalization in multi-step syntheses.
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