4,4,5,5-Tetramethyl-2-(2,4,6-trifluorophenyl)-1,3,2-dioxaborolane
98%
- Product Code: 241560
CAS:
325143-04-2
| Molecular Weight: | Molecular Formula: | ||
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 269.0±40.0℃(Predicted) | |
| Density: | 1.17±0.1g/ml(Predicted) | Storage Condition: | 2-8℃, 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 electron-deficient aryl group enhances reactivity and stability, making it particularly effective in coupling with aryl and heteroaryl halides under mild conditions. Commonly employed in pharmaceutical and agrochemical research for constructing biaryl scaffolds. Also utilized in materials science for preparing conjugated polymers and organic electronic materials due to its reliable performance in palladium-catalyzed transformations.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿850.00 |
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| 5.000 G | 10-20 days | ฿3,780.00 |
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| 25.000 G | 10-20 days | ฿16,800.00 |
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4,4,5,5-Tetramethyl-2-(2,4,6-trifluorophenyl)-1,3,2-dioxaborolane
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 electron-deficient aryl group enhances reactivity and stability, making it particularly effective in coupling with aryl and heteroaryl halides under mild conditions. Commonly employed in pharmaceutical and agrochemical research for constructing biaryl scaffolds. Also utilized in materials science for preparing conjugated polymers and organic electronic materials due to its reliable performance in palladium-catalyzed transformations.
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