5-(4-(Bis(4-methoxyphenyl)amino)phenyl)thiophene-2-carbaldehyde
98%
- Product Code: 151237
CAS:
1343425-46-6
| Molecular Weight: | 415.50 g./mol | Molecular Formula: | C₂₅H₂₁NO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Used as an intermediate in organic synthesis, particularly in the preparation of conjugated organic materials for optoelectronic devices. It serves as a building block in the fabrication of organic semiconductors, including those used in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The aldehyde group allows for further functionalization via condensation reactions, enabling the extension of π-conjugated systems. Its triphenylamine-like structure contributes to good hole-transport properties, making it valuable in designing efficient charge-transport materials. Also employed in the synthesis of dyes and fluorescent probes due to its strong electron-donating characteristics and light-emitting behavior when incorporated into larger aromatic systems.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,600.00 |
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| 0.500 | 10-20 days | ฿8,800.00 |
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| 1.000 | 10-20 days | ฿10,760.00 |
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| 5.000 | 10-20 days | ฿41,730.00 |
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5-(4-(Bis(4-methoxyphenyl)amino)phenyl)thiophene-2-carbaldehyde
Used as an intermediate in organic synthesis, particularly in the preparation of conjugated organic materials for optoelectronic devices. It serves as a building block in the fabrication of organic semiconductors, including those used in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The aldehyde group allows for further functionalization via condensation reactions, enabling the extension of π-conjugated systems. Its triphenylamine-like structure contributes to good hole-transport properties, making it valuable in designing efficient charge-transport materials. Also employed in the synthesis of dyes and fluorescent probes due to its strong electron-donating characteristics and light-emitting behavior when incorporated into larger aromatic systems.
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| Stable in pH range | - |
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