1-Cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
95%
- Product Code: 123902
CAS:
2123477-78-9
| Molecular Weight: | 234.1 g./mol | Molecular Formula: | C₁₂H₁₉BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18250655 | |
| Melting Point: | Boiling Point: | 354.3±15.0 °C(Predicted) | |
| Density: | 1.16±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, protected from light |
Product Description:
This compound is primarily used in organic synthesis as a key intermediate in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. It is particularly useful in the construction of biaryl compounds, which are common structural motifs in many drugs and biologically active compounds. Additionally, its pyrazole moiety is often leveraged in medicinal chemistry for designing molecules with potential therapeutic effects, such as anti-inflammatory, anticancer, or antimicrobial properties. The cyclopropyl group further enhances its utility by contributing to the stability and bioavailability of the resulting compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,700.00 |
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1-Cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
This compound is primarily used in organic synthesis as a key intermediate in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. It is particularly useful in the construction of biaryl compounds, which are common structural motifs in many drugs and biologically active compounds. Additionally, its pyrazole moiety is often leveraged in medicinal chemistry for designing molecules with potential therapeutic effects, such as anti-inflammatory, anticancer, or antimicrobial properties. The cyclopropyl group further enhances its utility by contributing to the stability and bioavailability of the resulting compounds.
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