4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER
98%
- Product Code: 90521
CAS:
214360-65-3
| Molecular Weight: | 272.07 g./mol | Molecular Formula: | C₁₃H₁₆BF₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is widely used in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for constructing complex organic molecules, particularly in the synthesis of aromatic compounds. Additionally, it is employed in the development of liquid crystals and organic electronic materials, where precise molecular architecture is crucial. Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the final products, making it valuable in drug discovery and development.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| APPEARANCE | White to off-white solid |
| Proton NMR Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿280.00 |
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| 1.000 | 10-20 days | ฿480.00 |
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| 5.000 | 10-20 days | ฿1,520.00 |
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| 25.000 | 10-20 days | ฿5,840.00 |
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4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER
This compound is widely used in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for constructing complex organic molecules, particularly in the synthesis of aromatic compounds. Additionally, it is employed in the development of liquid crystals and organic electronic materials, where precise molecular architecture is crucial. Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the final products, making it valuable in drug discovery and development.
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