2-[(Trimethylsilyl)ethynyl]thiophene
97%
- Product Code: 239930
Alias:
2-Trimethylsilicethiophen
CAS:
40231-03-6
| Molecular Weight: | 180.34 g./mol | Molecular Formula: | C₉H₁₂SSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427125 | |
| Melting Point: | Boiling Point: | 100 °C | |
| Density: | 1.09 g/mL at 25 °C(lit.) | Storage Condition: | Room temperature, flammable area |
Product Description:
Used in organic semiconductor materials, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl group enables efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to build thiophene-based electronic materials with tunable band gaps and improved charge carrier mobility. Also used in the development of fluorescent sensors and optoelectronic devices due to its luminescent properties when incorporated into larger aromatic systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | $108.90 |
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| 25g | 10-20 days | $526.36 |
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| 1g | 10-20 days | $34.14 |
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2-[(Trimethylsilyl)ethynyl]thiophene
Used in organic semiconductor materials, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl group enables efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to build thiophene-based electronic materials with tunable band gaps and improved charge carrier mobility. Also used in the development of fluorescent sensors and optoelectronic devices due to its luminescent properties when incorporated into larger aromatic systems.
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