1-Bromo-4-Chloro-9H-Carbazole

99%

Reagent Code: #151496
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CAS Number 2127377-11-9

science Other reagents with same CAS 2127377-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.55 g/mol
Formula C₁₂H₇BrClN
thermostat Physical Properties
Boiling Point 434.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.709±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in organic semiconductor materials due to its electron-rich aromatic structure, enabling applications in OLEDs and organic photovoltaics. Serves as a building block in the synthesis of pharmaceuticals and dyes, particularly in developing compounds with biological activity. Commonly employed in cross-coupling reactions like Suzuki and Buchwald-Hartwig to form C–C and C–N bonds for advanced functional materials. Its halogen positions allow selective functionalization, making it valuable in research and development of electroactive compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,050.00
inventory 5g
10-20 days ฿11,970.00

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1-Bromo-4-Chloro-9H-Carbazole
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Used in organic semiconductor materials due to its electron-rich aromatic structure, enabling applications in OLEDs and organic photovoltaics. Serves as a building block in the synthesis of pharmaceuticals and dyes, particularly in developing compounds with biological activity. Commonly employed in cross-coupling reactions like Suzuki and Buchwald-Hartwig to form C–C and C–N bonds for advanced functional materials. Its halogen positions allow selective functionalization, making it valuable in research an

Used in organic semiconductor materials due to its electron-rich aromatic structure, enabling applications in OLEDs and organic photovoltaics. Serves as a building block in the synthesis of pharmaceuticals and dyes, particularly in developing compounds with biological activity. Commonly employed in cross-coupling reactions like Suzuki and Buchwald-Hartwig to form C–C and C–N bonds for advanced functional materials. Its halogen positions allow selective functionalization, making it valuable in research and development of electroactive compounds.

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