2,2'-(Perfluoro-1,4-phenylene)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
98%
- Product Code: 131713
CAS:
1192055-60-9
| Molecular Weight: | 402 g./mol | Molecular Formula: | C₁₈H₂₄B₂F₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12964091 | |
| Melting Point: | Boiling Point: | 417.1±45.0 °C(Predicted) | |
| Density: | 1.19±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic compounds. Its boronate ester groups facilitate efficient carbon-carbon bond formation, particularly in the development of electron-deficient arenes for advanced materials. Commonly applied in the preparation of conjugated polymers and organic semiconductors where high electron affinity and thermal stability are required. The perfluorinated aromatic core enhances oxidative stability and influences molecular packing in thin-film devices, making it valuable in organic electronics such as OLEDs and OFETs. Also employed in medicinal chemistry for constructing fluorinated scaffolds with improved metabolic stability and bioavailability.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €48.28 |
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| 0.250 | 10-20 days | €81.88 |
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| 1.000 | 10-20 days | €212.84 |
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2,2'-(Perfluoro-1,4-phenylene)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
Used as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic compounds. Its boronate ester groups facilitate efficient carbon-carbon bond formation, particularly in the development of electron-deficient arenes for advanced materials. Commonly applied in the preparation of conjugated polymers and organic semiconductors where high electron affinity and thermal stability are required. The perfluorinated aromatic core enhances oxidative stability and influences molecular packing in thin-film devices, making it valuable in organic electronics such as OLEDs and OFETs. Also employed in medicinal chemistry for constructing fluorinated scaffolds with improved metabolic stability and bioavailability.
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