2-Fluoro-5-(trifluoromethyl)phenylboronic acid
98%
- Product Code: 67398
Alias:
2-Fluoro-5-trifluoromethylphenylboronic acid
CAS:
352535-96-7
| Molecular Weight: | 207.92 g./mol | Molecular Formula: | C₇H₅BF₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03701538 | |
| Melting Point: | 104-109 °C(lit.) | Boiling Point: | 262℃ |
| Density: | 1.44 | Storage Condition: | 2~8°C |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex aromatic structures. Its applications extend to the pharmaceutical industry, where it is utilized in the development of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is employed in material science for the synthesis of advanced polymers and organic electronic materials. The presence of fluorine atoms enhances its reactivity and stability, making it suitable for high-performance applications in various chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 104 109? |
| PurityGC | 98 100% |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿850.00 |
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| 5.000 | 10-20 days | ฿2,170.00 |
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| 25.000 | 10-20 days | ฿9,920.00 |
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2-Fluoro-5-(trifluoromethyl)phenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex aromatic structures. Its applications extend to the pharmaceutical industry, where it is utilized in the development of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is employed in material science for the synthesis of advanced polymers and organic electronic materials. The presence of fluorine atoms enhances its reactivity and stability, making it suitable for high-performance applications in various chemical processes.
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