5'-(4-Bromophenyl)-m-terphenyl

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Reagent Code: #147726
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CAS Number 116941-52-7

science Other reagents with same CAS 116941-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 385.3 g/mol
Formula C₂₄H₁₇Br
badge Registry Numbers
MDL Number MFCD26407506
thermostat Physical Properties
Melting Point 150°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic electronics as a semiconducting material in thin-film transistors and organic light-emitting diodes (OLEDs). Its rigid, conjugated structure enhances charge carrier mobility and thermal stability, making it suitable for high-performance optoelectronic devices. Also employed as a building block in the synthesis of liquid crystals and other functional materials for display technologies. Its bromine functionality allows for further chemical modification via cross-coupling reactions, enabling tailored electronic properties in advanced materials research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,480.00
inventory 5g
10-20 days ฿5,520.00

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5'-(4-Bromophenyl)-m-terphenyl
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Used in organic electronics as a semiconducting material in thin-film transistors and organic light-emitting diodes (OLEDs). Its rigid, conjugated structure enhances charge carrier mobility and thermal stability, making it suitable for high-performance optoelectronic devices. Also employed as a building block in the synthesis of liquid crystals and other functional materials for display technologies. Its bromine functionality allows for further chemical modification via cross-coupling reactions, enabling

Used in organic electronics as a semiconducting material in thin-film transistors and organic light-emitting diodes (OLEDs). Its rigid, conjugated structure enhances charge carrier mobility and thermal stability, making it suitable for high-performance optoelectronic devices. Also employed as a building block in the synthesis of liquid crystals and other functional materials for display technologies. Its bromine functionality allows for further chemical modification via cross-coupling reactions, enabling tailored electronic properties in advanced materials research.

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