4,4,5,5-Tetramethyl-2-(4-(trifluoromethyl)benzyl)-1,3,2-dioxaborolane
97%
- Product Code: 240916
CAS:
475250-46-5
| Molecular Weight: | 286.1 g./mol | Molecular Formula: | C₁₄H₁₈BF₃O₂ |
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| Density: | Storage Condition: | 2-8°C |
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 acts as a stable organoboron precursor, facilitating coupling with aryl halides under palladium catalysis. Particularly valuable for introducing trifluoromethyl-substituted aryl groups into complex molecules, enhancing metabolic stability and lipophilicity in drug design. Also employed in materials science for constructing conjugated organic frameworks and functionalized aromatic systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿1,070.00 |
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| 0.250 G | 10-20 days | ฿2,170.00 |
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| 1.000 G | 10-20 days | ฿5,500.00 |
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| 5.000 G | 10-20 days | ฿26,310.00 |
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4,4,5,5-Tetramethyl-2-(4-(trifluoromethyl)benzyl)-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 acts as a stable organoboron precursor, facilitating coupling with aryl halides under palladium catalysis. Particularly valuable for introducing trifluoromethyl-substituted aryl groups into complex molecules, enhancing metabolic stability and lipophilicity in drug design. Also employed in materials science for constructing conjugated organic frameworks and functionalized aromatic systems.
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