3,5-Bis(trifluoromethyl)phenylboronic acid
97%
- Product Code: 89947
Alias:
3,5-bis(trifluoromethyl)phenylboronic acid; 3,5-bis(trifluoromethyl)phenylboronic acid, 3,5-bis(trifluoromethyl)phenylboronic acid
CAS:
73852-19-4
| Molecular Weight: | 257.93 g./mol | Molecular Formula: | C₈H₅BF₆O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00051850 | |
| Melting Point: | 217-220 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
3,5-Bis(trifluoromethyl)phenylboronic 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's trifluoromethyl groups enhance its reactivity and stability, allowing it to act as an efficient coupling partner in the synthesis of complex organic molecules. Additionally, it is employed in the development of boron-based drugs and as a building block in medicinal chemistry for creating biologically active compounds. Its unique structure also makes it useful in the preparation of specialty chemicals and polymers.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97-100 |
| Melting point | 219-226 |
| APPEARANCE | White to Off-white Powder crystals |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿750.00 |
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| 25.000 | 10-20 days | ฿2,980.00 |
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| 100.000 | 10-20 days | ฿12,300.00 |
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3,5-Bis(trifluoromethyl)phenylboronic acid
3,5-Bis(trifluoromethyl)phenylboronic 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's trifluoromethyl groups enhance its reactivity and stability, allowing it to act as an efficient coupling partner in the synthesis of complex organic molecules. Additionally, it is employed in the development of boron-based drugs and as a building block in medicinal chemistry for creating biologically active compounds. Its unique structure also makes it useful in the preparation of specialty chemicals and polymers.
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