2,8-Bis(trifluoromethoxy)dibenzothiophene

≥98.0%(HPLC)

Reagent Code: #141599
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CAS Number 2833773-74-1

science Other reagents with same CAS 2833773-74-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.25 g/mol
Formula C₁₄H₆F₆O₂S
thermostat Physical Properties
Melting Point 92 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance materials for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its electron-deficient aromatic structure enhances charge transport properties and improves device efficiency. The presence of trifluoromethoxy groups increases thermal stability and influences molecular packing, which is beneficial for thin-film device fabrication. Also explored in pharmaceutical research for its potential bioisosteric properties due to fluorine substitution.

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inventory 1g
10-20 days ฿6,900.00

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2,8-Bis(trifluoromethoxy)dibenzothiophene
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Used as an intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance materials for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its electron-deficient aromatic structure enhances charge transport properties and improves device efficiency. The presence of trifluoromethoxy groups increases thermal stability and influences molecular packing, which is beneficial for thin-film device fabrication. Also explored in pharmaceutical rese

Used as an intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance materials for organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its electron-deficient aromatic structure enhances charge transport properties and improves device efficiency. The presence of trifluoromethoxy groups increases thermal stability and influences molecular packing, which is beneficial for thin-film device fabrication. Also explored in pharmaceutical research for its potential bioisosteric properties due to fluorine substitution.

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