4-Methoxy-2-(trifluoromethyl)phenylboronic Acid Pinacol Ester
98%
- Product Code: 208563
CAS:
1218790-37-4
| Molecular Weight: | 302.100 g./mol | Molecular Formula: | C₁₄H₁₈BF₃O₃ |
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| EC Number: | MDL Number: | MFCD09746197 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronic ester group provides enhanced stability and handling compared to the corresponding boronic acid, making it suitable for pharmaceutical and agrochemical research. The electron-donating methoxy and electron-withdrawing trifluoromethyl groups on the aromatic ring allow for fine-tuning of electronic properties in target compounds, particularly in the development of bioactive molecules and functional materials. Commonly employed in late-stage functionalization due to its compatibility with various functional groups under palladium catalysis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿4,030.00 |
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| 5g | 10-20 days | ฿14,080.00 |
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| 25g | 10-20 days | ฿49,290.00 |
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4-Methoxy-2-(trifluoromethyl)phenylboronic Acid Pinacol Ester
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronic ester group provides enhanced stability and handling compared to the corresponding boronic acid, making it suitable for pharmaceutical and agrochemical research. The electron-donating methoxy and electron-withdrawing trifluoromethyl groups on the aromatic ring allow for fine-tuning of electronic properties in target compounds, particularly in the development of bioactive molecules and functional materials. Commonly employed in late-stage functionalization due to its compatibility with various functional groups under palladium catalysis.
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