(4-Propoxy-3-(trifluoromethyl)phenyl)boronic acid
98%
- Product Code: 129482
CAS:
1162257-45-5
| Molecular Weight: | 248.01 g./mol | Molecular Formula: | C₁₀H₁₂BF₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20231450 | |
| Melting Point: | Boiling Point: | 346.8±52.0 °C(Predicted) | |
| Density: | 1.27±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable for constructing complex aromatic systems. The presence of a trifluoromethyl group enhances electron-withdrawing properties, which can improve metabolic stability and bioavailability in drug candidates. Commonly employed in the synthesis of bioactive molecules and functional materials requiring fluorinated aromatic motifs.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,230.00 |
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| 1g | 10-20 days | ฿3,370.00 |
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| 5g | 10-20 days | ฿11,870.00 |
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(4-Propoxy-3-(trifluoromethyl)phenyl)boronic acid
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable for constructing complex aromatic systems. The presence of a trifluoromethyl group enhances electron-withdrawing properties, which can improve metabolic stability and bioavailability in drug candidates. Commonly employed in the synthesis of bioactive molecules and functional materials requiring fluorinated aromatic motifs.
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