Trimethyl(thiophen-2-yl)stannane
95%
- Product Code: 58478
CAS:
37496-13-2
| Molecular Weight: | 246.95 g./mol | Molecular Formula: | C₇H₁₂SSn |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 301-303 °C(Solv: N,N-dimethylformamide (68-12-2)) | Boiling Point: | 91 °C(Press: 19 Torr) |
| Density: | 1.4021 g/cm3 | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
Trimethyl(thiophen-2-yl)stannane is primarily utilized in organic synthesis as a reagent for the introduction of thiophene groups into various molecules. It is particularly valuable in cross-coupling reactions, such as the Stille coupling, where it facilitates the formation of carbon-carbon bonds between thiophene and other aromatic or heteroaromatic compounds. This makes it a key component in the synthesis of complex organic materials, including conjugated polymers, which are essential in the development of organic semiconductors, photovoltaic cells, and light-emitting diodes (LEDs). Additionally, it is employed in the preparation of pharmaceuticals and agrochemicals, where thiophene derivatives often exhibit significant biological activity. Its role in creating tailored molecular structures underscores its importance in advanced material science and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,610.00 |
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Trimethyl(thiophen-2-yl)stannane
Trimethyl(thiophen-2-yl)stannane is primarily utilized in organic synthesis as a reagent for the introduction of thiophene groups into various molecules. It is particularly valuable in cross-coupling reactions, such as the Stille coupling, where it facilitates the formation of carbon-carbon bonds between thiophene and other aromatic or heteroaromatic compounds. This makes it a key component in the synthesis of complex organic materials, including conjugated polymers, which are essential in the development of organic semiconductors, photovoltaic cells, and light-emitting diodes (LEDs). Additionally, it is employed in the preparation of pharmaceuticals and agrochemicals, where thiophene derivatives often exhibit significant biological activity. Its role in creating tailored molecular structures underscores its importance in advanced material science and medicinal chemistry.
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