3,6-Dibromo-9-(2-ethylhexyl)carbazole

≥98%

Reagent Code: #174324
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CAS Number 173063-52-0

science Other reagents with same CAS 173063-52-0

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scatter_plot Molecular Information
Weight 437.22 g/mol
Formula C₂₀H₂₃Br₂N
badge Registry Numbers
MDL Number MFCD18252907
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in organic semiconductor materials, particularly in the development of high-performance OLEDs (organic light-emitting diodes) and perovskite solar cells. Its brominated carbazole structure enables efficient functionalization through cross-coupling reactions, allowing the synthesis of tailored hole-transport materials and host compounds. The presence of the 2-ethylhexyl group enhances solubility in organic solvents, facilitating solution-based processing techniques like spin-coating and inkjet printing for thin-film device fabrication. Exhibits good thermal stability and hole-transport properties, making it valuable in improving device efficiency and longevity in optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,210.00
inventory 5g
10-20 days ฿17,930.00
inventory 1g
10-20 days ฿5,560.00

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3,6-Dibromo-9-(2-ethylhexyl)carbazole
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Used as a key intermediate in organic semiconductor materials, particularly in the development of high-performance OLEDs (organic light-emitting diodes) and perovskite solar cells. Its brominated carbazole structure enables efficient functionalization through cross-coupling reactions, allowing the synthesis of tailored hole-transport materials and host compounds. The presence of the 2-ethylhexyl group enhances solubility in organic solvents, facilitating solution-based processing techniques like spin-coa

Used as a key intermediate in organic semiconductor materials, particularly in the development of high-performance OLEDs (organic light-emitting diodes) and perovskite solar cells. Its brominated carbazole structure enables efficient functionalization through cross-coupling reactions, allowing the synthesis of tailored hole-transport materials and host compounds. The presence of the 2-ethylhexyl group enhances solubility in organic solvents, facilitating solution-based processing techniques like spin-coating and inkjet printing for thin-film device fabrication. Exhibits good thermal stability and hole-transport properties, making it valuable in improving device efficiency and longevity in optoelectronic applications.

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