(2-Methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid
97%
- Product Code: 89057
CAS:
1067228-89-0
| Molecular Weight: | 287.95 g./mol | Molecular Formula: | C₉H₇BF₆O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27756648 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This chemical is primarily 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 organic molecules. Its trifluoromethyl groups enhance the reactivity and stability of the boronic acid, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive compounds and functional materials due to its ability to introduce specific structural motifs into target molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,510.00 |
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| 0.250 | 10-20 days | ฿5,346.00 |
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| 1.000 | 10-20 days | ฿14,292.00 |
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(2-Methoxy-4,6-bis(trifluoromethyl)phenyl)boronic acid
This chemical is primarily 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 organic molecules. Its trifluoromethyl groups enhance the reactivity and stability of the boronic acid, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive compounds and functional materials due to its ability to introduce specific structural motifs into target molecules.
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