3-Bromo-9-(4-chlorophenyl)-9H-carbazole

95%

Reagent Code: #154710
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CAS Number 1151816-79-3

science Other reagents with same CAS 1151816-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.64 g/mol
Formula C₁₈H₁₁BrClN
badge Registry Numbers
MDL Number MFCD30469066
thermostat Physical Properties
Boiling Point 482.5±41.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.47±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of functional materials for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its halogenated structure allows for further cross-coupling reactions, such as Suzuki coupling, enabling the construction of complex conjugated systems. Commonly employed in the development of hole-transport materials and host compounds in emissive layers due to its favorable thermal stability and electronic properties. Also utilized in research settings for synthesizing carbazole-based polymers and small molecules with tailored luminescent and charge-transport characteristics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,510.00
inventory 250mg
10-20 days ฿4,240.00
inventory 1g
10-20 days ฿13,990.00

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3-Bromo-9-(4-chlorophenyl)-9H-carbazole
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Used as an intermediate in organic synthesis, particularly in the preparation of functional materials for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its halogenated structure allows for further cross-coupling reactions, such as Suzuki coupling, enabling the construction of complex conjugated systems. Commonly employed in the development of hole-transport materials and host compounds in emissive layers due to its favorable thermal stability and e

Used as an intermediate in organic synthesis, particularly in the preparation of functional materials for optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its halogenated structure allows for further cross-coupling reactions, such as Suzuki coupling, enabling the construction of complex conjugated systems. Commonly employed in the development of hole-transport materials and host compounds in emissive layers due to its favorable thermal stability and electronic properties. Also utilized in research settings for synthesizing carbazole-based polymers and small molecules with tailored luminescent and charge-transport characteristics.

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