4-(Naphthalen-1-yl)-N-(4-(naphthalen-2-yl)phenyl)aniline

95%

Reagent Code: #214696
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CAS Number 1446448-95-8

science Other reagents with same CAS 1446448-95-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 421.53 g/mol
Formula C₃₂H₂₃N
thermostat Physical Properties
Boiling Point 620.9±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.189±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a hole-transporting material in organic light-emitting diodes (OLEDs). It helps improve device efficiency by facilitating the movement of positive charges in the emissive layer. Commonly found in blue OLEDs due to its suitable energy levels and thermal stability. Also applied in organic photovoltaics and perovskite solar cells as an interfacial layer to enhance charge extraction. Its rigid aromatic structure contributes to high glass transition temperature, supporting stable thin-film formation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿890.00
inventory 1g
10-20 days ฿2,670.00
inventory 5g
10-20 days ฿9,050.00

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4-(Naphthalen-1-yl)-N-(4-(naphthalen-2-yl)phenyl)aniline
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Used as a hole-transporting material in organic light-emitting diodes (OLEDs). It helps improve device efficiency by facilitating the movement of positive charges in the emissive layer. Commonly found in blue OLEDs due to its suitable energy levels and thermal stability. Also applied in organic photovoltaics and perovskite solar cells as an interfacial layer to enhance charge extraction. Its rigid aromatic structure contributes to high glass transition temperature, supporting stable thin-film formation.<

Used as a hole-transporting material in organic light-emitting diodes (OLEDs). It helps improve device efficiency by facilitating the movement of positive charges in the emissive layer. Commonly found in blue OLEDs due to its suitable energy levels and thermal stability. Also applied in organic photovoltaics and perovskite solar cells as an interfacial layer to enhance charge extraction. Its rigid aromatic structure contributes to high glass transition temperature, supporting stable thin-film formation.

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