5,5′-Bis(trimethylstannyl)-2,2′-bithiophene

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Reagent Code: #146912
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CAS Number 143367-56-0

science Other reagents with same CAS 143367-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 491.87 g/mol
Formula C₁₄H₂₂S₂Sn₂
badge Registry Numbers
MDL Number MFCD21363046
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its stannyl functional groups enable efficient Stille coupling reactions, allowing for precise construction of complex π-conjugated systems. The bithiophene core contributes to strong charge carrier mobility and light absorption in the visible range, making it valuable in designing high-performance semiconducting materials. It is especially favored in research settings for developing solution-processable organic semiconductors due to its reactivity and stability during polymerization.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,540.00
inventory 1g
10-20 days ฿5,930.00
inventory 5g
10-20 days ฿26,700.00

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5,5′-Bis(trimethylstannyl)-2,2′-bithiophene
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Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its stannyl functional groups enable efficient Stille coupling reactions, allowing for precise construction of complex π-conjugated systems. The bithiophene core contributes to strong charge carrier mobility and light absorption in the visible range, making it valuable in designing high-performance semicond

Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its stannyl functional groups enable efficient Stille coupling reactions, allowing for precise construction of complex π-conjugated systems. The bithiophene core contributes to strong charge carrier mobility and light absorption in the visible range, making it valuable in designing high-performance semiconducting materials. It is especially favored in research settings for developing solution-processable organic semiconductors due to its reactivity and stability during polymerization.

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