3,6-Diiodo-9-phenylcarbazole

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Reagent Code: #174326
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CAS Number 57103-21-6

science Other reagents with same CAS 57103-21-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 495.1 g/mol
Formula C₁₈H₁₁I₂N
badge Registry Numbers
MDL Number MFCD11521285
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of optoelectronic materials. Commonly employed in the development of hole-transport materials for organic light-emitting diodes (OLEDs) and perovskite solar cells due to its excellent thermal stability and favorable electronic properties. Its iodinated structure allows for further functionalization via cross-coupling reactions, making it valuable in the construction of complex conjugated systems for semiconductor applications. Also explored in photoredox catalysis and as a building block in the synthesis of fluorescent dyes and sensors.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿148.50
inventory 1g
10-20 days ฿165.00
inventory 5g
10-20 days ฿1,150.00

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3,6-Diiodo-9-phenylcarbazole
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Used as a key intermediate in organic synthesis, particularly in the preparation of optoelectronic materials. Commonly employed in the development of hole-transport materials for organic light-emitting diodes (OLEDs) and perovskite solar cells due to its excellent thermal stability and favorable electronic properties. Its iodinated structure allows for further functionalization via cross-coupling reactions, making it valuable in the construction of complex conjugated systems for semiconductor application

Used as a key intermediate in organic synthesis, particularly in the preparation of optoelectronic materials. Commonly employed in the development of hole-transport materials for organic light-emitting diodes (OLEDs) and perovskite solar cells due to its excellent thermal stability and favorable electronic properties. Its iodinated structure allows for further functionalization via cross-coupling reactions, making it valuable in the construction of complex conjugated systems for semiconductor applications. Also explored in photoredox catalysis and as a building block in the synthesis of fluorescent dyes and sensors.

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