3,3'-(2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-fluorene-9,9-diyl)bis(N,N-dimethylpropan-1-amine)
98%
- Product Code: 59891
CAS:
953390-94-8
| Molecular Weight: | 588.447 g./mol | Molecular Formula: | C₃₅H₅₄B₂N₂O₄ |
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| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate for constructing complex organic molecules. Its boronate ester groups make it highly effective in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorene-based structure contributes to its use in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its ability to enhance charge transport and stability. The dimethylpropan-1-amine groups further improve solubility and reactivity, making it a versatile component in various chemical processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $64.42 |
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| 0.500 | 10-20 days | $146.53 |
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| 1.000 | 10-20 days | $243.86 |
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3,3'-(2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-fluorene-9,9-diyl)bis(N,N-dimethylpropan-1-amine)
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate for constructing complex organic molecules. Its boronate ester groups make it highly effective in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorene-based structure contributes to its use in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its ability to enhance charge transport and stability. The dimethylpropan-1-amine groups further improve solubility and reactivity, making it a versatile component in various chemical processes.
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