tert-Butyl 3-(cyanomethyl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)azetidine-1-carboxylate
98%
- Product Code: 44561
CAS:
1153949-15-5
| Molecular Weight: | 388.2600 g./mol | Molecular Formula: | C₁₉H₂₉BN₄O₄ |
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| EC Number: | MDL Number: | MFCD28401390 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules, leveraging its boronic ester functionality for Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, its azetidine and pyrazole moieties make it valuable in designing molecules with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a versatile tool in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,467.00 |
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tert-Butyl 3-(cyanomethyl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)azetidine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules, leveraging its boronic ester functionality for Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the synthesis of biologically active compounds. Additionally, its azetidine and pyrazole moieties make it valuable in designing molecules with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a versatile tool in medicinal chemistry and drug discovery processes.
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