4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)sulfonyl)phenyl)-1,3,2-dioxaborolane
97%
- Product Code: 244476
CAS:
648904-89-6
| Molecular Weight: | 336.13 g./mol | Molecular Formula: | C₁₃H₁₆BF₃O₄S |
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| EC Number: | MDL Number: | MFCD28969495 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Widely used in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its electron-deficient aryl group enhances reactivity and stability, making it valuable for constructing complex aromatic systems. It is particularly useful in late-stage functionalization due to its tolerance of various functional groups and compatibility with palladium catalysts. Additionally, it acts as a building block in materials science for designing organic electronic materials and conjugated polymers.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $852.26 |
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4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)sulfonyl)phenyl)-1,3,2-dioxaborolane
Widely used in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its electron-deficient aryl group enhances reactivity and stability, making it valuable for constructing complex aromatic systems. It is particularly useful in late-stage functionalization due to its tolerance of various functional groups and compatibility with palladium catalysts. Additionally, it acts as a building block in materials science for designing organic electronic materials and conjugated polymers.
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