(1-(tert-Butoxycarbonyl)-6-chloro-1H-indol-2-yl)boronic acid
98%
- Product Code: 36123
CAS:
352359-22-9
| Molecular Weight: | 295.5300 g./mol | Molecular Formula: | C₁₃H₁₅BClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08689539 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, while the boronic acid moiety facilitates the formation of carbon-carbon bonds. Its application is significant in the development of indole-based compounds, which are widely studied for their biological activities, including potential use in drug discovery for treating various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,206.00 |
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(1-(tert-Butoxycarbonyl)-6-chloro-1H-indol-2-yl)boronic acid
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, while the boronic acid moiety facilitates the formation of carbon-carbon bonds. Its application is significant in the development of indole-based compounds, which are widely studied for their biological activities, including potential use in drug discovery for treating various diseases.
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