(2-(3-Fluoropropoxy)-4-(trifluoromethoxy)phenyl)boronic acid
98%
- Product Code: 89004
CAS:
1704073-53-9
| Molecular Weight: | 282 g./mol | Molecular Formula: | C₁₀H₁₁BF₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384336 | |
| 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. These reactions are crucial for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group serves as a key functional moiety, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, its fluorinated substituents enhance its stability and reactivity, making it valuable in the development of fluorine-containing compounds, which are often sought after for their unique properties in drug discovery and material science.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿83,930.00 |
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(2-(3-Fluoropropoxy)-4-(trifluoromethoxy)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group serves as a key functional moiety, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, its fluorinated substituents enhance its stability and reactivity, making it valuable in the development of fluorine-containing compounds, which are often sought after for their unique properties in drug discovery and material science.
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