2,5-Dibromo-3-cyclohexylthiophene

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Reagent Code: #174508
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CAS Number 302912-44-3

science Other reagents with same CAS 302912-44-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.07 g/mol
Formula C₁₀H₁₂Br₂S
badge Registry Numbers
MDL Number MFCD02683539
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for efficient cross-coupling reactions, such as Stille or Suzuki coupling, enabling the construction of complex conjugated systems. The cyclohexyl group enhances solubility and influences molecular packing, which can improve thin-film morphology and charge carrier mobility in semiconductor devices. Commonly employed in research settings to develop high-performance organic semiconducting materials.

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inventory 200mg
10-20 days ฿8,740.00

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2,5-Dibromo-3-cyclohexylthiophene
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Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for efficient cross-coupling reactions, such as Stille or Suzuki coupling, enabling the construction of complex conjugated systems. The cyclohexyl group enhances solubility and influences molecular packing, which can improve thin-film morphology and charge carrier mobility in semiconductor dev

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated structure allows for efficient cross-coupling reactions, such as Stille or Suzuki coupling, enabling the construction of complex conjugated systems. The cyclohexyl group enhances solubility and influences molecular packing, which can improve thin-film morphology and charge carrier mobility in semiconductor devices. Commonly employed in research settings to develop high-performance organic semiconducting materials.

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