4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
97%
- Product Code: 241246
CAS:
1255309-13-7
| Molecular Weight: | 293.17 g./mol | Molecular Formula: | C₁₈H₂₀BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16996079 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing conjugated organic materials. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of organic semiconductors, OLEDs (organic light-emitting diodes), and pharmaceutical intermediates. The carbazole moiety contributes hole-transport properties and thermal stability, which are advantageous in optoelectronic devices. It is also employed in the synthesis of functional polymers and small molecules for use in photovoltaics and sensors.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿630.00 |
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| 1.000 G | 10-20 days | ฿1,730.00 |
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| 5.000 G | 10-20 days | ฿7,380.00 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing conjugated organic materials. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of organic semiconductors, OLEDs (organic light-emitting diodes), and pharmaceutical intermediates. The carbazole moiety contributes hole-transport properties and thermal stability, which are advantageous in optoelectronic devices. It is also employed in the synthesis of functional polymers and small molecules for use in photovoltaics and sensors.
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