tert-Butyl (R)-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)carbamate
97%
- Product Code: 104170
CAS:
578729-05-2
| Molecular Weight: | 347.26 g./mol | Molecular Formula: | C₁₉H₃₀BNO₄ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a key intermediate in the development of boron-containing compounds, which are essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, a critical step in the synthesis of complex organic molecules. Additionally, the tert-butyl carbamate protecting group ensures selective reactivity during multi-step synthetic processes, enhancing the efficiency of target molecule production. Its application is crucial in the design and synthesis of biologically active compounds, including potential drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,000.00 |
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| 0.250 | 10-20 days | ฿14,940.00 |
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| 1.000 | 10-20 days | ฿28,710.00 |
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tert-Butyl (R)-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)carbamate
This chemical is primarily used in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a key intermediate in the development of boron-containing compounds, which are essential in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed to form carbon-carbon bonds, a critical step in the synthesis of complex organic molecules. Additionally, the tert-butyl carbamate protecting group ensures selective reactivity during multi-step synthetic processes, enhancing the efficiency of target molecule production. Its application is crucial in the design and synthesis of biologically active compounds, including potential drug candidates.
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