tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
95%
- Product Code: 83088
CAS:
1883598-68-2
| Molecular Weight: | 357.2516 g./mol | Molecular Formula: | C₂₀H₂₈BNO₄ |
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| EC Number: | MDL Number: | MFCD14155741 | |
| 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 functional group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the synthesis of indole derivatives, which are crucial in developing biologically active compounds, including potential drugs. Additionally, it serves as a building block in materials science for creating advanced organic materials with specific properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿3,762.00 |
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| 0.100 | 10-20 days | ฿11,196.00 |
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tert-butyl 5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the synthesis of indole derivatives, which are crucial in developing biologically active compounds, including potential drugs. Additionally, it serves as a building block in materials science for creating advanced organic materials with specific properties.
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