4-(2-(tert-Butoxycarbonyl(cyclopropyl)amino)ethoxy)-3-fluorophenylboronic acid
98%
- Product Code: 90336
CAS:
1704064-17-4
| Molecular Weight: | 339.17 g./mol | Molecular Formula: | C₁₆H₂₃BFNO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400180 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, while the cyclopropyl and fluorine substituents can influence the electronic and steric properties of the resulting products. This chemical is often employed in the development of biologically active compounds, where its structural features contribute to enhanced selectivity and efficacy.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | €911.50 |
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4-(2-(tert-Butoxycarbonyl(cyclopropyl)amino)ethoxy)-3-fluorophenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, while the cyclopropyl and fluorine substituents can influence the electronic and steric properties of the resulting products. This chemical is often employed in the development of biologically active compounds, where its structural features contribute to enhanced selectivity and efficacy.
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