Ethyl 4-(trimethylsilyl)but-3-ynoate

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Reagent Code: #131364
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CAS Number 53059-24-8

science Other reagents with same CAS 53059-24-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.31 g/mol
Formula C₉H₁₆O₂Si
badge Registry Numbers
MDL Number MFCD34476324
thermostat Physical Properties
Boiling Point 192.1±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.923±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a key building block in organic synthesis, particularly in the preparation of conjugated systems and functionalized alkynes. Its silyl-protected alkyne group allows for selective deprotection and further coupling reactions, making it valuable in pharmaceutical and agrochemical synthesis. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to construct carbon-carbon bonds. Also utilized in materials science for developing organic electronic compounds due to its ability to extend π-conjugation when incorporated into larger molecular frameworks.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,710.00
inventory 250mg
10-20 days ฿14,790.00

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Ethyl 4-(trimethylsilyl)but-3-ynoate
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Used as a key building block in organic synthesis, particularly in the preparation of conjugated systems and functionalized alkynes. Its silyl-protected alkyne group allows for selective deprotection and further coupling reactions, making it valuable in pharmaceutical and agrochemical synthesis. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to construct carbon-carbon bonds. Also utilized in materials science for developing organic electronic compounds due to its

Used as a key building block in organic synthesis, particularly in the preparation of conjugated systems and functionalized alkynes. Its silyl-protected alkyne group allows for selective deprotection and further coupling reactions, making it valuable in pharmaceutical and agrochemical synthesis. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to construct carbon-carbon bonds. Also utilized in materials science for developing organic electronic compounds due to its ability to extend π-conjugation when incorporated into larger molecular frameworks.

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