4,4,5,5-Tetramethyl-2-(3-(9-phenyl-9H-fluoren-9-yl)phenyl)-1,3,2-dioxaborolane
98%
- Product Code: 238208
CAS:
1260032-45-8
| Molecular Weight: | 444.37 g./mol | Molecular Formula: | C₃₁H₂₉BO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 556.2±29.0 °C(Predicted) | |
| Density: | 1.17±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, inert gas |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in the preparation of conjugated organic materials for optoelectronic applications such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound’s bulky fluorenyl and phenyl groups enhance steric stability and influence electronic properties in the resulting polymers or small molecules. Its borolane moiety provides high reactivity and selectivity under palladium catalysis, making it suitable for constructing advanced functional materials in academic and industrial research settings.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 250mg | 10-20 days | ฿1,440.00 |
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| 1g | 10-20 days | ฿3,830.00 |
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| 5g | 10-20 days | ฿13,310.00 |
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4,4,5,5-Tetramethyl-2-(3-(9-phenyl-9H-fluoren-9-yl)phenyl)-1,3,2-dioxaborolane
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in the preparation of conjugated organic materials for optoelectronic applications such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound’s bulky fluorenyl and phenyl groups enhance steric stability and influence electronic properties in the resulting polymers or small molecules. Its borolane moiety provides high reactivity and selectivity under palladium catalysis, making it suitable for constructing advanced functional materials in academic and industrial research settings.
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