N-(2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-phenylacetamide
95%
- Product Code: 83678
CAS:
2045409-68-3
| Molecular Weight: | 367.2464 g./mol | Molecular Formula: | C₂₁H₂₆BNO₄ |
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| EC Number: | MDL Number: | MFCD32206525 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it serves as a key building block in the preparation of advanced materials, such as organic semiconductors or polymers, where precise molecular architecture is required. Its application extends to medicinal chemistry, where it aids in the creation of targeted therapies and drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿3,672.00 |
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| 0.100 | 10-20 days | ฿10,998.00 |
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N-(2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-phenylacetamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it serves as a key building block in the preparation of advanced materials, such as organic semiconductors or polymers, where precise molecular architecture is required. Its application extends to medicinal chemistry, where it aids in the creation of targeted therapies and drug discovery efforts.
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