4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-N,N-bis[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]aniline
98%
- Product Code: 218029
CAS:
267221-90-9
| Molecular Weight: | 623.2200 g./mol | Molecular Formula: | C₃₆H₄₈B₃NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28098209 | |
| Melting Point: | 334-335℃ | Boiling Point: | 702.3±55.0℃(Predicted) |
| Density: | 1.12±0.1g/ml(Predicted) | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers and small molecules for optoelectronic devices. Its multiple boronate ester groups enable cross-coupling reactions, especially Suzuki-Miyaura couplings, allowing the construction of complex π-conjugated systems. It is particularly valuable in the development of hole-transport materials and emissive layers in organic light-emitting diodes (OLEDs). Additionally, it finds use in the preparation of donor-acceptor type polymers for organic photovoltaics (OPVs), where its structural design enhances charge carrier mobility and film morphology. The compound’s multifunctional boronate structure also supports the formation of covalent organic frameworks (COFs) with tunable electronic properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1g | 10-20 days | $55.47 |
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| 5g | 10-20 days | $217.49 |
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4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-N,N-bis[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]aniline
Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers and small molecules for optoelectronic devices. Its multiple boronate ester groups enable cross-coupling reactions, especially Suzuki-Miyaura couplings, allowing the construction of complex π-conjugated systems. It is particularly valuable in the development of hole-transport materials and emissive layers in organic light-emitting diodes (OLEDs). Additionally, it finds use in the preparation of donor-acceptor type polymers for organic photovoltaics (OPVs), where its structural design enhances charge carrier mobility and film morphology. The compound’s multifunctional boronate structure also supports the formation of covalent organic frameworks (COFs) with tunable electronic properties.
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