2-(Cyclohexen-1-yl)ethynyl-trimethyl-silane
98%
- Product Code: 166507
CAS:
17988-44-2
| Molecular Weight: | 178.35 g./mol | Molecular Formula: | C₁₁H₁₈Si |
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used primarily as a synthetic intermediate in organic chemistry, this compound serves in the construction of complex molecules through alkyne-based transformations. Its ethynyl group participates in coupling reactions, such as Sonogashira coupling, enabling the formation of carbon-carbon bonds in pharmaceuticals and agrochemicals. The trimethylsilyl group acts as a protecting group for the alkyne, allowing selective deprotection under mild conditions to reveal terminal alkynes for further functionalization. It is also employed in materials science for synthesizing conjugated systems and molecular wires due to the rigid cyclohexenyl backbone and linear alkyne spacer. Its stability and reactivity profile make it valuable in multi-step synthesis where controlled reactivity is essential.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,130.00 |
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| 1g | 10-20 days | ฿5,660.00 |
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| 5g | 10-20 days | ฿17,000.00 |
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| 10g | 10-20 days | ฿28,320.00 |
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| 250mg | 10-20 days | ฿2,270.00 |
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2-(Cyclohexen-1-yl)ethynyl-trimethyl-silane
Used primarily as a synthetic intermediate in organic chemistry, this compound serves in the construction of complex molecules through alkyne-based transformations. Its ethynyl group participates in coupling reactions, such as Sonogashira coupling, enabling the formation of carbon-carbon bonds in pharmaceuticals and agrochemicals. The trimethylsilyl group acts as a protecting group for the alkyne, allowing selective deprotection under mild conditions to reveal terminal alkynes for further functionalization. It is also employed in materials science for synthesizing conjugated systems and molecular wires due to the rigid cyclohexenyl backbone and linear alkyne spacer. Its stability and reactivity profile make it valuable in multi-step synthesis where controlled reactivity is essential.
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