3-(1-Methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-1H-pyrrole-2,5-dione
95%
- Product Code: 73798
CAS:
125313-92-0
Molecular Weight: | 400.39722 g./mol | Molecular Formula: | C₂₂H₁₆N₄O₄ |
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EC Number: | MDL Number: | ||
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Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic electronics due to its unique electronic properties. It is often employed as a key component in the development of organic semiconductors, which are essential for creating flexible and lightweight electronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells (OPVs). Its structure allows for efficient charge transport, making it suitable for use in thin-film transistors and other electronic components. Additionally, its photophysical properties make it a candidate for use in sensors and imaging applications, where it can detect specific analytes or emit light under certain conditions. Researchers also explore its potential in dye-sensitized solar cells (DSSCs) to enhance energy conversion efficiency.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.010 | 10-20 days | £345.14 |
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0.025 | 10-20 days | £678.06 |
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0.100 | 10-20 days | £2,645.28 |
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3-(1-Methyl-1H-indol-3-yl)-4-(1-methyl-6-nitro-1H-indol-3-yl)-1H-pyrrole-2,5-dione
This compound is primarily utilized in the field of organic electronics due to its unique electronic properties. It is often employed as a key component in the development of organic semiconductors, which are essential for creating flexible and lightweight electronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells (OPVs). Its structure allows for efficient charge transport, making it suitable for use in thin-film transistors and other electronic components. Additionally, its photophysical properties make it a candidate for use in sensors and imaging applications, where it can detect specific analytes or emit light under certain conditions. Researchers also explore its potential in dye-sensitized solar cells (DSSCs) to enhance energy conversion efficiency.
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