(4-Ethynylphenyl)trimethylsilane
≥98%
- Product Code: 88013
CAS:
16116-92-0
| Molecular Weight: | 174.32 g./mol | Molecular Formula: | C₁₁H₁₄Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26394823 | |
| Melting Point: | Boiling Point: | 75°C/4mmHg(lit.) | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in organic synthesis, particularly in the development of advanced materials and pharmaceuticals. It serves as a key building block in cross-coupling reactions, such as Sonogashira coupling, which is essential for creating carbon-carbon bonds in complex molecules. Its ethynyl group allows for the introduction of alkyne functionalities into organic frameworks, making it valuable in the synthesis of conjugated polymers, molecular wires, and optoelectronic materials. Additionally, the trimethylsilyl group provides protection for the ethynyl moiety during multi-step synthetic processes, ensuring selective reactivity. This chemical is also employed in the preparation of bioactive compounds and drug candidates, where its structural features contribute to the development of molecules with specific pharmacological properties. Its versatility makes it a crucial reagent in both academic research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Pale yellow Clear Liquid |
| PURITY | 98-100 |
| SPECIFIC GRAVITY 2020 | 0.9000-0.9040 |
| REFRACTIVE INDEX N20D | 1.5240-1.5280 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $26.70 |
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| 0.200 | 10-20 days | $85.81 |
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(4-Ethynylphenyl)trimethylsilane
This compound is primarily used in organic synthesis, particularly in the development of advanced materials and pharmaceuticals. It serves as a key building block in cross-coupling reactions, such as Sonogashira coupling, which is essential for creating carbon-carbon bonds in complex molecules. Its ethynyl group allows for the introduction of alkyne functionalities into organic frameworks, making it valuable in the synthesis of conjugated polymers, molecular wires, and optoelectronic materials. Additionally, the trimethylsilyl group provides protection for the ethynyl moiety during multi-step synthetic processes, ensuring selective reactivity. This chemical is also employed in the preparation of bioactive compounds and drug candidates, where its structural features contribute to the development of molecules with specific pharmacological properties. Its versatility makes it a crucial reagent in both academic research and industrial applications.
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