4,4,5,5-Tetramethyl-2-(4-(2,2,2-trifluoroethoxy)phenyl)-1,3,2-dioxaborolane
98%
- Product Code: 244185
CAS:
886528-42-3
| Molecular Weight: | 302.1 g./mol | Molecular Formula: | C₁₄H₁₈BF₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22418017 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, inert gas |
Product Description:
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boron-containing structure facilitates coupling with aryl halides under palladium catalysis, making it valuable for constructing biaryl systems found in active pharmaceutical ingredients. The electron-withdrawing trifluoroethoxy group enhances reactivity and stability, improving coupling efficiency in complex molecule assembly. Commonly employed in late-stage functionalization due to its tolerance of various functional groups and reliable performance in both research and industrial settings.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $148.19 |
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| 1.000 | 10-20 days | $471.56 |
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| 5.000 | 10-20 days | $1,648.55 |
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| 0.100 | 10-20 days | $86.64 |
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4,4,5,5-Tetramethyl-2-(4-(2,2,2-trifluoroethoxy)phenyl)-1,3,2-dioxaborolane
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boron-containing structure facilitates coupling with aryl halides under palladium catalysis, making it valuable for constructing biaryl systems found in active pharmaceutical ingredients. The electron-withdrawing trifluoroethoxy group enhances reactivity and stability, improving coupling efficiency in complex molecule assembly. Commonly employed in late-stage functionalization due to its tolerance of various functional groups and reliable performance in both research and industrial settings.
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