4,4,5,5-Tetramethyl-2-[4-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)phenyl]-1,3,2-dioxaborolane
95%
- Product Code: 243547
CAS:
620595-02-0
| Molecular Weight: | 332.25 g./mol | Molecular Formula: | C₁₉H₂₉BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22495442 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic rings. Its key role is as a boronic ester derivative, offering enhanced stability and reactivity compared to boronic acids. It serves as a building block for preparing conjugated organic materials, including those used in pharmaceuticals, agrochemicals, and advanced materials like organic light-emitting diodes (OLEDs) and semiconductors. The presence of dual dioxaborolane groups allows for sequential or selective coupling reactions, making it valuable in the synthesis of complex molecular architectures.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $46.40 |
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| 5.000 | 10-20 days | $152.45 |
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4,4,5,5-Tetramethyl-2-[4-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)phenyl]-1,3,2-dioxaborolane
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic rings. Its key role is as a boronic ester derivative, offering enhanced stability and reactivity compared to boronic acids. It serves as a building block for preparing conjugated organic materials, including those used in pharmaceuticals, agrochemicals, and advanced materials like organic light-emitting diodes (OLEDs) and semiconductors. The presence of dual dioxaborolane groups allows for sequential or selective coupling reactions, making it valuable in the synthesis of complex molecular architectures.
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