5,5'-Dibromo-4,4'-didodecyl-2,2'-bithiophene

98%

Reagent Code: #173818
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CAS Number 753470-95-0

science Other reagents with same CAS 753470-95-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 660.6900000000001 g/mol
Formula C₃₂H₅₂Br₂S₂
badge Registry Numbers
MDL Number MFCD24539450
thermostat Physical Properties
Melting Point 56-60 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated bithiophene core enables efficient palladium-catalyzed coupling reactions, facilitating the construction of high-performance donor-acceptor copolymers. The long dodecyl side chains improve solubility in organic solvents, which enhances processability and film-forming properties in solution-based fabrication techniques. This compound contributes to tuning the electronic properties and morphology of active layers in organic electronic devices, leading to improved charge carrier mobility and device efficiency.

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inventory 5g
10-20 days ฿16,380.00

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5,5'-Dibromo-4,4'-didodecyl-2,2'-bithiophene
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Used as a key intermediate in the synthesis of conjugated polymers for organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated bithiophene core enables efficient palladium-catalyzed coupling reactions, facilitating the construction of high-performance donor-acceptor copolymers. The long dodecyl side chains improve solubility in organic solvents, which enhances processability and film-forming properties in solution-based fabrication

Used as a key intermediate in the synthesis of conjugated polymers for organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated bithiophene core enables efficient palladium-catalyzed coupling reactions, facilitating the construction of high-performance donor-acceptor copolymers. The long dodecyl side chains improve solubility in organic solvents, which enhances processability and film-forming properties in solution-based fabrication techniques. This compound contributes to tuning the electronic properties and morphology of active layers in organic electronic devices, leading to improved charge carrier mobility and device efficiency.

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