Di-tert-butyl 3,6-bis(5-bromothiophen-2-yl)-1,4-dioxopyrrolo[3,4-c]pyrrole-2,5(1H,4H)-dicarboxylate
97%
- Product Code: 59894
CAS:
1046864-84-9
| Molecular Weight: | 658.389 g./mol | Molecular Formula: | C₂₄H₂₂Br₂N₂O₆S₂ |
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| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This chemical is primarily utilized in the development of organic electronic materials, particularly in the synthesis of conjugated polymers and small molecules for optoelectronic applications. Its structure, featuring bromothiophene and pyrrolo[3,4-c]pyrrole units, makes it a valuable building block for creating materials with desirable electronic properties. It is often employed in the fabrication of organic semiconductors used in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). The bromine atoms facilitate further functionalization through cross-coupling reactions, enabling the design of tailored materials with optimized performance for specific electronic devices. Additionally, its electron-deficient core contributes to enhancing charge transport properties, making it suitable for high-performance electronic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €671.95 |
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Di-tert-butyl 3,6-bis(5-bromothiophen-2-yl)-1,4-dioxopyrrolo[3,4-c]pyrrole-2,5(1H,4H)-dicarboxylate
This chemical is primarily utilized in the development of organic electronic materials, particularly in the synthesis of conjugated polymers and small molecules for optoelectronic applications. Its structure, featuring bromothiophene and pyrrolo[3,4-c]pyrrole units, makes it a valuable building block for creating materials with desirable electronic properties. It is often employed in the fabrication of organic semiconductors used in organic light-emitting diodes (OLEDs), organic photovoltaics (OPVs), and field-effect transistors (OFETs). The bromine atoms facilitate further functionalization through cross-coupling reactions, enabling the design of tailored materials with optimized performance for specific electronic devices. Additionally, its electron-deficient core contributes to enhancing charge transport properties, making it suitable for high-performance electronic applications.
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