1-Isopropyl-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
98%
- Product Code: 201164
CAS:
2446483-84-5
| Molecular Weight: | 250.14 g./mol | Molecular Formula: | C₁₃H₂₃BN₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
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. It is especially useful for introducing the 1-isopropyl-4-methyl-1H-pyrazole moiety into target structures, which can enhance biological activity or modulate physicochemical properties in drug discovery programs. The stability and reactivity profile of this reagent support its use in both small-scale research and late-stage functionalization during development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿15,930.00 |
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| 250mg | 10-20 days | ฿26,540.00 |
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| 1g | 10-20 days | ฿53,080.00 |
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1-Isopropyl-4-methyl-5-(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. It is especially useful for introducing the 1-isopropyl-4-methyl-1H-pyrazole moiety into target structures, which can enhance biological activity or modulate physicochemical properties in drug discovery programs. The stability and reactivity profile of this reagent support its use in both small-scale research and late-stage functionalization during development.
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