5,12-Dibromo-2,9-bis(2-octyldodecyl)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone

97%

Reagent Code: #177577
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CAS Number 1100243-37-5

science Other reagents with same CAS 1100243-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1109.20 g/mol
Formula C₆₄H₈₈Br₂N₂O₄
badge Registry Numbers
MDL Number MFCD30607293
thermostat Physical Properties
Boiling Point 996.8±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.199±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a high-performance organic semiconductor in flexible electronics and organic field-effect transistors (OFETs). Exhibits excellent charge carrier mobility and stability under ambient conditions, making it suitable for printed electronics and large-area sensor arrays. Its branched alkyl side chains enhance solubility in common organic solvents, enabling solution-processable device fabrication. Also explored in n-type organic photovoltaics due to its strong electron-accepting properties and broad light absorption in the visible to near-infrared range.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,380.00
inventory 250mg
10-20 days ฿9,130.00
inventory 1g
10-20 days ฿26,690.00

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5,12-Dibromo-2,9-bis(2-octyldodecyl)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone
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Used as a high-performance organic semiconductor in flexible electronics and organic field-effect transistors (OFETs). Exhibits excellent charge carrier mobility and stability under ambient conditions, making it suitable for printed electronics and large-area sensor arrays. Its branched alkyl side chains enhance solubility in common organic solvents, enabling solution-processable device fabrication. Also explored in n-type organic photovoltaics due to its strong electron-accepting properties and broad li

Used as a high-performance organic semiconductor in flexible electronics and organic field-effect transistors (OFETs). Exhibits excellent charge carrier mobility and stability under ambient conditions, making it suitable for printed electronics and large-area sensor arrays. Its branched alkyl side chains enhance solubility in common organic solvents, enabling solution-processable device fabrication. Also explored in n-type organic photovoltaics due to its strong electron-accepting properties and broad light absorption in the visible to near-infrared range.

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