9,9-Di-n-octylfluorene-2,7-diboronic acid bis(pinacol) ester
98%
- Product Code: 94150
Alias:
9,9-Dioctylfluorene-2,7-diboronic acid pinacol ester; 2,7-bis(4,4,5,5-tetramethyl-1,3-dioxo-2-boryl )-9,9-dioctylfluorene; 2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9 -Di-n-octylfluorene; 9,9-Di-n-octylfluorene-2,7-diboronic acid dipinacid;
CAS:
196207-58-6
| Molecular Weight: | 642.57 g./mol | Molecular Formula: | C₄₁H₆₄B₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16294554 | |
| Melting Point: | 129ºC | Boiling Point: | 701.622ºC at 760 mmHg |
| Density: | 1.01g/cm3 | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is widely used in organic electronics, particularly in the synthesis of conjugated polymers for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure allows it to act as a key monomer in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of high-performance materials with excellent charge transport properties. Additionally, it is employed in the development of sensors and optoelectronic devices due to its ability to form stable and efficient π-conjugated systems. Its solubility in organic solvents also makes it suitable for solution-processing techniques, which are essential for large-scale manufacturing of flexible electronic devices.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Off white Crystal - Powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿820.00 |
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| 5.000 | 10-20 days | ฿3,060.00 |
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| 25.000 | 10-20 days | ฿11,990.00 |
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| 100.000 | 10-20 days | ฿44,660.00 |
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9,9-Di-n-octylfluorene-2,7-diboronic acid bis(pinacol) ester
This compound is widely used in organic electronics, particularly in the synthesis of conjugated polymers for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its structure allows it to act as a key monomer in Suzuki-Miyaura cross-coupling reactions, facilitating the creation of high-performance materials with excellent charge transport properties. Additionally, it is employed in the development of sensors and optoelectronic devices due to its ability to form stable and efficient π-conjugated systems. Its solubility in organic solvents also makes it suitable for solution-processing techniques, which are essential for large-scale manufacturing of flexible electronic devices.
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