tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
≥95%
- Product Code: 121433
CAS:
893441-86-6
| Molecular Weight: | 343.23 g./mol | Molecular Formula: | C₁₉H₂₆BNO₄ |
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| EC Number: | MDL Number: | MFCD14155783 | |
| Melting Point: | Boiling Point: | 454.6±37.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it serves as a building block in the preparation of indole derivatives, which are important in the creation of biologically active compounds, including potential drug candidates. Its stability and reactivity make it a useful tool in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €14.48 |
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| 0.250 | 10-20 days | €22.32 |
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| 1.000 | 10-20 days | €66.72 |
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| 5.000 | 10-20 days | €320.30 |
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tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
This compound is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it serves as a building block in the preparation of indole derivatives, which are important in the creation of biologically active compounds, including potential drug candidates. Its stability and reactivity make it a useful tool in medicinal chemistry research.
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