(1-(tert-Butoxycarbonyl)-6-fluoro-1H-indol-2-yl)boronic acid
98%
- Product Code: 39715
CAS:
1000068-26-7
| Molecular Weight: | 279.0700 g./mol | Molecular Formula: | C₁₃H₁₅BFNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953519 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex molecules, especially in pharmaceutical research. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable for constructing indole-based compounds. These compounds are often explored for their potential biological activities, including drug development for treating various diseases. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating controlled synthesis processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €66.96 |
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(1-(tert-Butoxycarbonyl)-6-fluoro-1H-indol-2-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex molecules, especially in pharmaceutical research. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable for constructing indole-based compounds. These compounds are often explored for their potential biological activities, including drug development for treating various diseases. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating controlled synthesis processes.
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