trans,trans-1,4-Diphenyl-1,3-butadiene
98%
- Product Code: 67761
Alias:
trans,trans-1,4-diphenyl-1,3-butadiene β,β′-distyryl
CAS:
538-81-8
| Molecular Weight: | 206.28 g./mol | Molecular Formula: | C₁₆H₁₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00004791 | |
| Melting Point: | 150-152 °C(lit.) | Boiling Point: | 350 °C(lit.) |
| Density: | Storage Condition: | room temperature |
Product Description:
Trans,trans-1,4-Diphenyl-1,3-butadiene is primarily used in organic synthesis and material science. It serves as a key intermediate in the production of conjugated polymers and organic semiconductors, which are essential for developing flexible electronic devices, such as organic light-emitting diodes (OLEDs) and solar cells. Its extended π-conjugation system makes it valuable for studying photophysical properties and designing materials with specific optical and electronic characteristics. Additionally, it is utilized in research for understanding reaction mechanisms in organic chemistry, particularly in Diels-Alder reactions and polymerization processes.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 150 154? |
| PURITY GC | 98 100% |
| APPEARANCE | WHITE TO LIGHT YELLOW SOLID |
| INFRARED SPECTRUM | Conforms to Structure |
| SOLUBILITY | COLORLESS TO YELLOW TO TAN,CLEAR,C= 50 MG/ML,CHCL3 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿800.00 |
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| 25.000 | 10-20 days | ฿3,940.00 |
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trans,trans-1,4-Diphenyl-1,3-butadiene
Trans,trans-1,4-Diphenyl-1,3-butadiene is primarily used in organic synthesis and material science. It serves as a key intermediate in the production of conjugated polymers and organic semiconductors, which are essential for developing flexible electronic devices, such as organic light-emitting diodes (OLEDs) and solar cells. Its extended π-conjugation system makes it valuable for studying photophysical properties and designing materials with specific optical and electronic characteristics. Additionally, it is utilized in research for understanding reaction mechanisms in organic chemistry, particularly in Diels-Alder reactions and polymerization processes.
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