4-[N,N-Bis(4-bromophenyl)amino]benzaldehyde

98%

Reagent Code: #217780
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CAS Number 25069-38-9

science Other reagents with same CAS 25069-38-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.13 g/mol
Formula C₁₉H₁₃Br₂NO
badge Registry Numbers
MDL Number MFCD12547118
thermostat Physical Properties
Melting Point 156 °C
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used primarily as an intermediate in the synthesis of advanced organic semiconductors and electroactive materials. It serves as a building block in the preparation of hole-transport materials for organic light-emitting diodes (OLEDs) and perovskite solar cells due to its strong electron-donating properties and thermal stability. Its triphenylamine core with bromo substituents allows for further functionalization via cross-coupling reactions, enabling tailored modification for optoelectronic applications. Also employed in the development of nonlinear optical materials and fluorescent probes, where its extended conjugation and redox behavior enhance performance.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿810.00
250mg
10-20 days ฿1,800.00
1g
10-20 days ฿5,010.00
5g
10-20 days ฿17,990.00
4-[N,N-Bis(4-bromophenyl)amino]benzaldehyde
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Used primarily as an intermediate in the synthesis of advanced organic semiconductors and electroactive materials. It serves as a building block in the preparation of hole-transport materials for organic light-emitting diodes (OLEDs) and perovskite solar cells due to its strong electron-donating properties and thermal stability. Its triphenylamine core with bromo substituents allows for further functionalization via cross-coupling reactions, enabling tailored modification for optoelectronic applications.

Used primarily as an intermediate in the synthesis of advanced organic semiconductors and electroactive materials. It serves as a building block in the preparation of hole-transport materials for organic light-emitting diodes (OLEDs) and perovskite solar cells due to its strong electron-donating properties and thermal stability. Its triphenylamine core with bromo substituents allows for further functionalization via cross-coupling reactions, enabling tailored modification for optoelectronic applications. Also employed in the development of nonlinear optical materials and fluorescent probes, where its extended conjugation and redox behavior enhance performance.

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