4,6-di(2-thienyl)thieno[3,4-c][1,2,5]thiadiazole
97%
- Product Code: 45968
CAS:
150600-72-9
| Molecular Weight: | 308.46532 g./mol | Molecular Formula: | C₁₂H₈N₂S₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 157-158℃(Solv: hexane (110-54-3)) | Boiling Point: | 473.2±55.0℃(Predicted) |
| Density: | 1.70±0.1g/ml(Predicted) | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the development of organic electronic materials due to its unique conjugated structure, which facilitates efficient electron transport. It is commonly employed in the synthesis of organic semiconductors for applications such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ability to absorb light in the visible spectrum makes it suitable for use in light-harvesting systems, including solar cells. Additionally, its stability and electronic properties are leveraged in the design of electrochromic devices, which change color in response to an electric field. The compound’s thiophene-based structure also contributes to its use in creating conductive polymers and advanced materials for flexible electronics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿10,890.00 |
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| 1.000 | 10-20 days | ฿29,313.00 |
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4,6-di(2-thienyl)thieno[3,4-c][1,2,5]thiadiazole
This chemical is primarily utilized in the development of organic electronic materials due to its unique conjugated structure, which facilitates efficient electron transport. It is commonly employed in the synthesis of organic semiconductors for applications such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ability to absorb light in the visible spectrum makes it suitable for use in light-harvesting systems, including solar cells. Additionally, its stability and electronic properties are leveraged in the design of electrochromic devices, which change color in response to an electric field. The compound’s thiophene-based structure also contributes to its use in creating conductive polymers and advanced materials for flexible electronics.
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