N,9,9-Triphenyl-9H-fluoren-2-amine

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Reagent Code: #217671
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CAS Number 860465-14-1

science Other reagents with same CAS 860465-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.53 g/mol
Formula C₃₁H₂₃N
badge Registry Numbers
MDL Number MFCD30470208
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in organic electronics, this compound serves as a key building block in the synthesis of hole-transport materials for OLEDs (organic light-emitting diodes). Its rigid, conjugated structure enhances thermal stability and improves film-forming properties in device layers. It is also employed in the development of organic semiconductors and emissive layers due to its favorable electron-donating characteristics and high triplet energy, making it suitable for blue phosphorescent OLEDs. Additionally, derivatives are explored in perovskite solar cells as dopant-free hole-transport agents to improve device efficiency and stability.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿190.00
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿800.00
inventory 25g
10-20 days ฿3,390.00
inventory 100g
10-20 days ฿13,500.00

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N,9,9-Triphenyl-9H-fluoren-2-amine
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Used primarily in organic electronics, this compound serves as a key building block in the synthesis of hole-transport materials for OLEDs (organic light-emitting diodes). Its rigid, conjugated structure enhances thermal stability and improves film-forming properties in device layers. It is also employed in the development of organic semiconductors and emissive layers due to its favorable electron-donating characteristics and high triplet energy, making it suitable for blue phosphorescent OLEDs. Addition

Used primarily in organic electronics, this compound serves as a key building block in the synthesis of hole-transport materials for OLEDs (organic light-emitting diodes). Its rigid, conjugated structure enhances thermal stability and improves film-forming properties in device layers. It is also employed in the development of organic semiconductors and emissive layers due to its favorable electron-donating characteristics and high triplet energy, making it suitable for blue phosphorescent OLEDs. Additionally, derivatives are explored in perovskite solar cells as dopant-free hole-transport agents to improve device efficiency and stability.

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