3-[(Trimethylsilyl)ethynyl]thiophene

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Reagent Code: #239800
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Alias 3-(trimethylsilylalkynyl)thiophene
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CAS Number 130995-13-0

science Other reagents with same CAS 130995-13-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.34 g/mol
Formula C₉H₁₂SSi
badge Registry Numbers
MDL Number MFCD04039959
thermostat Physical Properties
Melting Point 36-41 °C(lit.)
Boiling Point 203.6±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.98 g/cm3
Storage Room temperature, light-proof, inert gas

description Product Description

Used in organic electronics as a building block for conjugated polymers and small molecules in organic semiconductors. Its ethynyl group enables coupling reactions, facilitating the synthesis of extended π-conjugated systems for use in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to construct thiophene-based electronic materials with tunable band gaps and improved charge transport properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,230.00
inventory 50g
10-20 days ฿28,030.00
inventory 5g
10-20 days ฿4,590.00
3-[(Trimethylsilyl)ethynyl]thiophene
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Used in organic electronics as a building block for conjugated polymers and small molecules in organic semiconductors. Its ethynyl group enables coupling reactions, facilitating the synthesis of extended π-conjugated systems for use in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to construct thioph

Used in organic electronics as a building block for conjugated polymers and small molecules in organic semiconductors. Its ethynyl group enables coupling reactions, facilitating the synthesis of extended π-conjugated systems for use in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to construct thiophene-based electronic materials with tunable band gaps and improved charge transport properties.

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