4-Fluorophenylboronic acid
98%
- Product Code: 90611
Alias:
4-fluorophenylboronic acid; p-fluorophenylboronic acid
CAS:
1765-93-1
| Molecular Weight: | 139.92 g./mol | Molecular Formula: | C₆H₆BFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00039136 | |
| Melting Point: | 262-265 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
4-Fluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its fluorophenyl group enhances the stability and reactivity of the boronic acid, making it a preferred choice in various catalytic processes. Additionally, it is utilized in the development of sensors and diagnostic reagents due to its ability to interact selectively with specific biological targets.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 97.5 100% |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿290.00 |
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| 5.000 | 10-20 days | ฿390.00 |
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| 25.000 | 10-20 days | ฿910.00 |
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| 100.000 | 10-20 days | ฿2,980.00 |
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| 500.000 | 10-20 days | ฿14,300.00 |
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4-Fluorophenylboronic acid
4-Fluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its fluorophenyl group enhances the stability and reactivity of the boronic acid, making it a preferred choice in various catalytic processes. Additionally, it is utilized in the development of sensors and diagnostic reagents due to its ability to interact selectively with specific biological targets.
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