(Cyclopropylethynyl)trimethylsilane
95%
- Product Code: 56565
CAS:
81166-84-9
| Molecular Weight: | 138.28 g./mol | Molecular Formula: | C₈H₁₄Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00671355 | |
| Melting Point: | Boiling Point: | 87 °C(Press: 103 Torr) | |
| Density: | 0.85±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, inert atmosphere |
Product Description:
Used primarily in organic synthesis as a building block for more complex molecules. It is particularly valuable in the preparation of cyclopropylacetylene derivatives, which are important intermediates in pharmaceuticals and agrochemicals. The trimethylsilyl group acts as a protective group, enhancing the stability and reactivity of the cyclopropylethynyl moiety during chemical reactions. This compound is also employed in the development of novel materials and in research involving cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds. Its unique structure makes it a versatile reagent in the synthesis of cyclopropane-containing compounds, which are often explored for their biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,008.00 |
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| 5.000 | 10-20 days | ฿3,159.00 |
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| 25.000 | 10-20 days | ฿9,531.00 |
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(Cyclopropylethynyl)trimethylsilane
Used primarily in organic synthesis as a building block for more complex molecules. It is particularly valuable in the preparation of cyclopropylacetylene derivatives, which are important intermediates in pharmaceuticals and agrochemicals. The trimethylsilyl group acts as a protective group, enhancing the stability and reactivity of the cyclopropylethynyl moiety during chemical reactions. This compound is also employed in the development of novel materials and in research involving cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds. Its unique structure makes it a versatile reagent in the synthesis of cyclopropane-containing compounds, which are often explored for their biological activity.
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