2-Bromo-13,13-Dimethyl-6H-Indeno[1,2-b]Anthracene-6,11(13H)-Dione

≥98%

Reagent Code: #147115
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CAS Number 1196107-73-9

science Other reagents with same CAS 1196107-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 403.27 g/mol
Formula C₂₃H₁₅BrO₂
thermostat Physical Properties
Melting Point 264 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of high-performance organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances charge carrier mobility and stability in thin-film devices. Also employed in the development of fluorescent dyes and sensors due to its strong light absorption and emission properties in the visible range. Its bromine functionality allows for further chemical modification via cross-coupling reactions, making it valuable in tailoring materials for optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,440.00
inventory 25g
10-20 days ฿12,170.00
inventory 100g
10-20 days ฿33,190.00

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2-Bromo-13,13-Dimethyl-6H-Indeno[1,2-b]Anthracene-6,11(13H)-Dione
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Used as a key intermediate in the synthesis of high-performance organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances charge carrier mobility and stability in thin-film devices. Also employed in the development of fluorescent dyes and sensors due to its strong light absorption and emission properties in the visible range. Its bromine functionality allows for further chemical modification via cross-coupling r

Used as a key intermediate in the synthesis of high-performance organic semiconductors, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its rigid, planar structure enhances charge carrier mobility and stability in thin-film devices. Also employed in the development of fluorescent dyes and sensors due to its strong light absorption and emission properties in the visible range. Its bromine functionality allows for further chemical modification via cross-coupling reactions, making it valuable in tailoring materials for optoelectronic applications.

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