2,5-Bis[(trimethylsilyl)ethynyl]thiophene

96%

Reagent Code: #147426
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CAS Number 79109-69-6

science Other reagents with same CAS 79109-69-6

blur_circular Chemical Specifications

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Weight 276.54 g/mol
Formula C₁₄H₂₀SSi₂
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MDL Number MFCD18207392
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key intermediate in organic semiconductor synthesis, particularly in the development of conjugated polymers and small molecules for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl groups enable efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl groups enhance solubility and stability during synthesis, allowing for better processability in thin-film device fabrication. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to build complex donor-acceptor structures with tunable electronic properties.

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inventory 200mg
10-20 days ฿4,460.00

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2,5-Bis[(trimethylsilyl)ethynyl]thiophene
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Used as a key intermediate in organic semiconductor synthesis, particularly in the development of conjugated polymers and small molecules for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl groups enable efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl groups enhance solubility and stability during synthesis, allowing for better processability in thin-film device fabrication. Commonly employed in Sonoga

Used as a key intermediate in organic semiconductor synthesis, particularly in the development of conjugated polymers and small molecules for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its ethynyl groups enable efficient coupling reactions, facilitating the construction of extended π-conjugated systems. The trimethylsilyl groups enhance solubility and stability during synthesis, allowing for better processability in thin-film device fabrication. Commonly employed in Sonogashira and other palladium-catalyzed cross-coupling reactions to build complex donor-acceptor structures with tunable electronic properties.

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