N-Phenyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)naphthalen-2-amine
98%
- Product Code: 131835
CAS:
1347758-75-1
| Molecular Weight: | 421.34 g./mol | Molecular Formula: | C₂₈H₂₈BNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 568.4±33.0 °C(Predicted) | |
| Density: | 1.16±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, inert gas |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated organic materials. It plays an important role in the development of organic semiconductors, particularly in the fabrication of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound’s boronate ester group enables efficient carbon-carbon bond formation, allowing for the construction of complex aromatic amine-based structures that exhibit good hole-transport properties. Its structural design supports thermal stability and film-forming ability, making it suitable for use in solution-processed electronic devices.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,040.00 |
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| 0.250 | 10-20 days | ฿5,180.00 |
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| 1.000 | 10-20 days | ฿13,970.00 |
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N-Phenyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)naphthalen-2-amine
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated organic materials. It plays an important role in the development of organic semiconductors, particularly in the fabrication of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound’s boronate ester group enables efficient carbon-carbon bond formation, allowing for the construction of complex aromatic amine-based structures that exhibit good hole-transport properties. Its structural design supports thermal stability and film-forming ability, making it suitable for use in solution-processed electronic devices.
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