2-[(Trimethylsilyl)ethynyl]thiophene

97%

Reagent Code: #239930
label
Alias 2-Trimethylsilicethiophen
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CAS Number 40231-03-6

science Other reagents with same CAS 40231-03-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.34 g/mol
Formula C₉H₁₂SSi
badge Registry Numbers
MDL Number MFCD03427125
thermostat Physical Properties
Boiling Point 100 °C
inventory_2 Storage & Handling
Density 1.09 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area

description Product Description

Used in organic semiconductor materials, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl group enables efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to build thiophene-based electronic materials with tunable band gaps and improved charge carrier mobility. Also used in the development of fluorescent sensors and optoelectronic devices due to its luminescent properties when incorporated into larger aromatic systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,520.00
inventory 25g
10-20 days ฿12,180.00
inventory 1g
10-20 days ฿790.00
2-[(Trimethylsilyl)ethynyl]thiophene
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Used in organic semiconductor materials, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl group enables efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to build thiophene-based electronic m

Used in organic semiconductor materials, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl group enables efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl group stabilizes the alkyne during synthesis and can be easily removed to enable further functionalization. Commonly employed in Sonogashira coupling reactions to build thiophene-based electronic materials with tunable band gaps and improved charge carrier mobility. Also used in the development of fluorescent sensors and optoelectronic devices due to its luminescent properties when incorporated into larger aromatic systems.

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