Phenyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methanone
97%
- Product Code: 40278
CAS:
1562244-79-4
| Molecular Weight: | 298.14466 g./mol | Molecular Formula: | C₁₆H₁₉BN₂O₃ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester reagent. Its structure, featuring a pyrazole ring and a boronate ester group, makes it a valuable intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronate ester moiety facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, it may be employed in the preparation of heterocyclic compounds, which are often found in bioactive molecules. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing and optimizing drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $239.26 |
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| 0.250 | 10-20 days | $399.24 |
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| 1.000 | 10-20 days | $1,061.09 |
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Phenyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methanone
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester reagent. Its structure, featuring a pyrazole ring and a boronate ester group, makes it a valuable intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronate ester moiety facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug discovery and material science. Additionally, it may be employed in the preparation of heterocyclic compounds, which are often found in bioactive molecules. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing and optimizing drug candidates.
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