Trimethyl((4-nitrophenyl)ethynyl)silane

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Reagent Code: #244625
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CAS Number 75867-38-8

science Other reagents with same CAS 75867-38-8

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scatter_plot Molecular Information
Weight 219.31 g/mol
Formula C₁₁H₁₃NO₂Si
badge Registry Numbers
MDL Number MFCD00555128
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated materials for optoelectronic devices. Its ethynyl group enables coupling reactions, making it valuable in constructing molecular wires and organic semiconductors. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to build extended π-systems. The nitrophenyl moiety provides a handle for further functionalization or acts as an electron-withdrawing group, influencing electronic properties in sensor design and nonlinear optical materials. Also utilized in surface modification of silicon-based materials due to the trimethylsilyl group, enhancing stability and compatibility in thin-film applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,690.00
inventory 5g
10-20 days ฿20,640.00
inventory 100mg
10-20 days ฿1,810.00
inventory 250mg
10-20 days ฿3,020.00
inventory 10g
10-20 days ฿30,050.00

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Trimethyl((4-nitrophenyl)ethynyl)silane
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Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated materials for optoelectronic devices. Its ethynyl group enables coupling reactions, making it valuable in constructing molecular wires and organic semiconductors. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to build extended π-systems. The nitrophenyl moiety provides a handle for further functionalization or acts as an electron-withdrawing group, influencing electroni

Used as a key intermediate in organic synthesis, particularly in the preparation of conjugated materials for optoelectronic devices. Its ethynyl group enables coupling reactions, making it valuable in constructing molecular wires and organic semiconductors. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to build extended π-systems. The nitrophenyl moiety provides a handle for further functionalization or acts as an electron-withdrawing group, influencing electronic properties in sensor design and nonlinear optical materials. Also utilized in surface modification of silicon-based materials due to the trimethylsilyl group, enhancing stability and compatibility in thin-film applications.

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