4-Bromo-N,N-bis(4-iodophenyl)aniline

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Reagent Code: #215426
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CAS Number 1266674-69-4

science Other reagents with same CAS 1266674-69-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 576.01 g/mol
Formula C₁₈H₁₂BrI₂N
thermostat Physical Properties
Boiling Point 546.7±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.050±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily in organic synthesis as an intermediate for pharmaceuticals and advanced materials. Serves as a building block in the preparation of conjugated organic compounds for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its halogen substituents enable cross-coupling reactions, particularly in palladium-catalyzed processes like Suzuki or Ullmann couplings, allowing the construction of complex aromatic systems. Also employed in the development of nonlinear optical materials due to its extended π-conjugation and electron-rich character.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,000.00
inventory 5g
10-20 days ฿10,000.00
inventory 10g
10-20 days ฿16,000.00
inventory 50g
10-20 days ฿67,990.00

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4-Bromo-N,N-bis(4-iodophenyl)aniline
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Used primarily in organic synthesis as an intermediate for pharmaceuticals and advanced materials. Serves as a building block in the preparation of conjugated organic compounds for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its halogen substituents enable cross-coupling reactions, particularly in palladium-catalyzed processes like Suzuki or Ullmann couplings, allowing the construction of complex aromatic systems. Also employed in the development of
Used primarily in organic synthesis as an intermediate for pharmaceuticals and advanced materials. Serves as a building block in the preparation of conjugated organic compounds for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its halogen substituents enable cross-coupling reactions, particularly in palladium-catalyzed processes like Suzuki or Ullmann couplings, allowing the construction of complex aromatic systems. Also employed in the development of nonlinear optical materials due to its extended π-conjugation and electron-rich character.
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