(11BR)-1,1,1-trifluoro-N-(4-oxido-2,6-di(phenanthren-9-yl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)methanesulfonamide

98%

  • Product Code: 70377
  CAS:    937028-51-8
Molecular Weight: 831.79 g./mol Molecular Formula: C₄₉H₂₉F₃NO₅PS
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: 1.54±0.1 g/cm3 Storage Condition: 2-8°C
Product Description: This chemical is primarily used in advanced materials research, particularly in the development of organic semiconductors and optoelectronic devices. Its unique structure, featuring phenanthrene and dioxaphosphepin moieties, makes it suitable for applications in organic light-emitting diodes (OLEDs) and photovoltaic cells. The compound's ability to facilitate electron transport and its stability under various conditions enhance the efficiency and durability of these devices. Additionally, it is explored in the synthesis of novel phosphorescent materials, which are crucial for high-performance displays and lighting technologies. Its trifluoromethanesulfonamide group also contributes to its potential use in catalysis, particularly in reactions requiring robust and electron-withdrawing ligands.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.010 10-20 days ฿9,882.00
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-
0.050 10-20 days ฿38,952.00
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-
(11BR)-1,1,1-trifluoro-N-(4-oxido-2,6-di(phenanthren-9-yl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)methanesulfonamide
This chemical is primarily used in advanced materials research, particularly in the development of organic semiconductors and optoelectronic devices. Its unique structure, featuring phenanthrene and dioxaphosphepin moieties, makes it suitable for applications in organic light-emitting diodes (OLEDs) and photovoltaic cells. The compound's ability to facilitate electron transport and its stability under various conditions enhance the efficiency and durability of these devices. Additionally, it is explored in the synthesis of novel phosphorescent materials, which are crucial for high-performance displays and lighting technologies. Its trifluoromethanesulfonamide group also contributes to its potential use in catalysis, particularly in reactions requiring robust and electron-withdrawing ligands.
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