tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline-1-carboxylate
98%
- Product Code: 48206
CAS:
837392-67-3
| Molecular Weight: | 345.2500 g./mol | Molecular Formula: | C₁₉H₂₈BNO₄ |
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| EC Number: | MDL Number: | MFCD12408237 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyl group provides stability and can be selectively removed under mild conditions, offering versatility in synthetic pathways. Its application is especially prominent in the development of indoline-based compounds, which are often explored for their biological activity in drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $142.39 |
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tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline-1-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyl group provides stability and can be selectively removed under mild conditions, offering versatility in synthetic pathways. Its application is especially prominent in the development of indoline-based compounds, which are often explored for their biological activity in drug discovery.
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