4-Fluoro-3-(trifluoromethyl)benzeneboronic acid
98%
- Product Code: 90599
Alias:
4-fluoro-3-(trifluoromethyl)phenylboronic acid
CAS:
182344-23-6
| Molecular Weight: | 207.92 g./mol | Molecular Formula: | C₇H₅BF₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07363787 | |
| Melting Point: | 170-174 | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables it to form stable bonds with various aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is utilized in the development of materials for electronic devices, such as organic light-emitting diodes (OLEDs), due to its ability to modify molecular structures for enhanced performance. Its fluorinated structure also contributes to its stability and reactivity in diverse chemical processes.
Product Specification:
| Test | Specification |
|---|---|
| PURITY HPLC | 98 100% |
| INFRARED SPECTRUM | Conforms to Structure |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿760.00 |
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| 25.000 | 10-20 days | ฿3,760.00 |
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4-Fluoro-3-(trifluoromethyl)benzeneboronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables it to form stable bonds with various aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is utilized in the development of materials for electronic devices, such as organic light-emitting diodes (OLEDs), due to its ability to modify molecular structures for enhanced performance. Its fluorinated structure also contributes to its stability and reactivity in diverse chemical processes.
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