Trimethyl((4-(trifluoromethyl)phenyl)ethynyl)silane

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Reagent Code: #244702
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CAS Number 40230-95-3

science Other reagents with same CAS 40230-95-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.316 g/mol
Formula C₁₂H₁₃F₃Si
thermostat Physical Properties
Boiling Point 80 °C at 0.1 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.029  g/cm3 at 25 °C(lit.)
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of advanced materials and pharmaceuticals. Its ethynyl group enables coupling reactions, such as Sonogashira cross-coupling, allowing the construction of conjugated systems important in electronic materials and liquid crystals. The trimethylsilyl group acts as a protecting group or solubility enhancer in synthetic pathways. The presence of the trifluoromethylphenyl moiety contributes electron-withdrawing properties, enhancing stability and influencing electronic characteristics in final products. Commonly applied in research settings for developing fluorinated compounds with potential biological activity or use in optoelectronic devices.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,370.00
inventory 1g
10-20 days ฿1,840.00

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Trimethyl((4-(trifluoromethyl)phenyl)ethynyl)silane
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Used as a key intermediate in organic synthesis, particularly in the preparation of advanced materials and pharmaceuticals. Its ethynyl group enables coupling reactions, such as Sonogashira cross-coupling, allowing the construction of conjugated systems important in electronic materials and liquid crystals. The trimethylsilyl group acts as a protecting group or solubility enhancer in synthetic pathways. The presence of the trifluoromethylphenyl moiety contributes electron-withdrawing properties, enhancin

Used as a key intermediate in organic synthesis, particularly in the preparation of advanced materials and pharmaceuticals. Its ethynyl group enables coupling reactions, such as Sonogashira cross-coupling, allowing the construction of conjugated systems important in electronic materials and liquid crystals. The trimethylsilyl group acts as a protecting group or solubility enhancer in synthetic pathways. The presence of the trifluoromethylphenyl moiety contributes electron-withdrawing properties, enhancing stability and influencing electronic characteristics in final products. Commonly applied in research settings for developing fluorinated compounds with potential biological activity or use in optoelectronic devices.

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