2-Fluoro-3-(trifluoromethyl)phenylboronic acid
97%
- Product Code: 67366
CAS:
157834-21-4
| Molecular Weight: | 207.92 g./mol | Molecular Formula: | C₇H₅BF₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07784336 | |
| Melting Point: | 56-58°C | Boiling Point: | 276.5°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound acts as a key intermediate for constructing complex molecules. It is valuable in pharmaceutical research for developing drug candidates, especially in modifying aromatic rings to enhance biological activity. Additionally, it finds application in material science for creating advanced polymers and organic electronic materials. Its unique fluorine substitution pattern contributes to improved stability and reactivity in various chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| 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 | ฿350.00 |
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| 1.000 | 10-20 days | ฿790.00 |
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| 5.000 | 10-20 days | ฿2,420.00 |
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2-Fluoro-3-(trifluoromethyl)phenylboronic acid
Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound acts as a key intermediate for constructing complex molecules. It is valuable in pharmaceutical research for developing drug candidates, especially in modifying aromatic rings to enhance biological activity. Additionally, it finds application in material science for creating advanced polymers and organic electronic materials. Its unique fluorine substitution pattern contributes to improved stability and reactivity in various chemical processes.
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