2-Fluoro-6-(trifluoromethyl)phenylboronic acid
97%
- Product Code: 79176
CAS:
313545-34-5
| Molecular Weight: | 207.92 g./mol | Molecular Formula: | C₇H₅BF₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07781239 | |
| Melting Point: | Boiling Point: | 267.288°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex molecules, often in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both fluorine and trifluoromethyl groups, enhances the reactivity and stability of the resulting compounds, making it valuable for designing drugs with improved metabolic stability and bioavailability. Additionally, it finds applications in material science, where it is used to synthesize advanced polymers and organic electronic materials. Its ability to introduce fluorine atoms into molecules is particularly advantageous in tuning the properties of materials for specific applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Tan Powder, Crystals or Crystalline Powder, and/or Chunks |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $11.40 |
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| 1.000 | 10-20 days | $30.00 |
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| 5.000 | 10-20 days | $121.21 |
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2-Fluoro-6-(trifluoromethyl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex molecules, often in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both fluorine and trifluoromethyl groups, enhances the reactivity and stability of the resulting compounds, making it valuable for designing drugs with improved metabolic stability and bioavailability. Additionally, it finds applications in material science, where it is used to synthesize advanced polymers and organic electronic materials. Its ability to introduce fluorine atoms into molecules is particularly advantageous in tuning the properties of materials for specific applications.
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