1-(2,7-Dibromospiro[fluorene-9,4'-piperidin]-1'-yl)ethanone

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Reagent Code: #175685
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CAS Number 1616114-00-1

science Other reagents with same CAS 1616114-00-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 435.15 g/mol
Formula C₁₉H₁₇Br₂NO
badge Registry Numbers
MDL Number MFCD28144724
thermostat Physical Properties
Boiling Point 568.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used in organic electronics as a building block for high-performance materials, particularly in the development of hole-transport layers for OLEDs and perovskite solar cells. Its spirofluorene core provides excellent thermal and oxidative stability, while the bromine substituents allow for further functionalization via cross-coupling reactions. The piperidinyl ketone moiety enhances electron-donating properties and supports film-forming characteristics in device fabrication. Commonly employed in research settings to tune energy levels and improve device efficiency in light-emitting diodes and photovoltaic cells.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,010.00
inventory 250mg
10-20 days ฿2,020.00

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1-(2,7-Dibromospiro[fluorene-9,4'-piperidin]-1'-yl)ethanone
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Used in organic electronics as a building block for high-performance materials, particularly in the development of hole-transport layers for OLEDs and perovskite solar cells. Its spirofluorene core provides excellent thermal and oxidative stability, while the bromine substituents allow for further functionalization via cross-coupling reactions. The piperidinyl ketone moiety enhances electron-donating properties and supports film-forming characteristics in device fabrication. Commonly employed in research

Used in organic electronics as a building block for high-performance materials, particularly in the development of hole-transport layers for OLEDs and perovskite solar cells. Its spirofluorene core provides excellent thermal and oxidative stability, while the bromine substituents allow for further functionalization via cross-coupling reactions. The piperidinyl ketone moiety enhances electron-donating properties and supports film-forming characteristics in device fabrication. Commonly employed in research settings to tune energy levels and improve device efficiency in light-emitting diodes and photovoltaic cells.

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