2,5-Dibromo-3-hexylthiophene
≥98%,GC
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Widely used in organic electronics, this compound serves as a key building block for conjugated polymers and small molecules in organic semiconductors. Its brominated structure allows for efficient coupling reactions, especially in Suzuki and Stille polymerizations, making it ideal for synthesizing donor-acceptor copolymers used in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The hexyl side chain enhances solubility in organic solvents, facilitating solution processing techniques like spin coating and inkjet printing. Due to its planar thiophene core and tunable electronic properties, it contributes to improved charge carrier mobility and light absorption in active layers of optoelectronic devices.
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