((4-((4-((4-(phenylethynyl)phenyl) ethynyl) phenyl)ethynyl)phenyl)ethynyl)triMethylsilane
≥95%
- Product Code: 214433
CAS:
484067-45-0
| Molecular Weight: | 474.677 g./mol | Molecular Formula: | C₃₅H₂₆Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22376617 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Sealed |
Product Description:
Used primarily in organic electronics and advanced materials research, this compound serves as a key building block for conjugated systems due to its extended π-conjugation. Its rigid, linear structure supports efficient electron delocalization, making it valuable in the synthesis of organic semiconductors, molecular wires, and light-emitting materials. It is also employed in the development of optoelectronic devices such as organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). The trimethylsilyl group enhances solubility and stability during synthetic processing, allowing for easier purification and integration into larger molecular architectures. Additionally, it acts as a precursor in Sonogashira coupling reactions to construct complex acetylene-based frameworks for nanotechnology and photonic applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | Ft427,587.01 |
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((4-((4-((4-(phenylethynyl)phenyl) ethynyl) phenyl)ethynyl)phenyl)ethynyl)triMethylsilane
Used primarily in organic electronics and advanced materials research, this compound serves as a key building block for conjugated systems due to its extended π-conjugation. Its rigid, linear structure supports efficient electron delocalization, making it valuable in the synthesis of organic semiconductors, molecular wires, and light-emitting materials. It is also employed in the development of optoelectronic devices such as organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). The trimethylsilyl group enhances solubility and stability during synthetic processing, allowing for easier purification and integration into larger molecular architectures. Additionally, it acts as a precursor in Sonogashira coupling reactions to construct complex acetylene-based frameworks for nanotechnology and photonic applications.
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