Diarylethers
Diarylethers are a class of organic compounds characterized by the presence of two aryl groups directly attached to an ether oxygen atom. These compounds are widely used in various applications due to their unique properties and structural versatility. Diarylethers exhibit excellent thermal stability, chemical resistance, and electrochemical characteristics, making them valuable for use in pharmaceuticals, polymers, and electronic materials.
In the pharmaceutical industry, diarylethers have been explored as potential drug candidates for treating diseases such as cancer and neurodegenerative disorders due to their ability to modulate enzyme activities. In polymer chemistry, these compounds are employed as crosslinking agents or additives that enhance mechanical properties and improve thermal stability of polymers. Additionally, diarylethers find applications in the electronics sector, where they serve as key components in organic light-emitting diodes (OLEDs) and liquid crystal displays (LCDs), contributing to their performance and durability.
The structural diversity of diarylethers allows for the modification of functional groups, enabling tailored properties that can be optimized for specific applications. Their synthesis involves various chemical reactions such as Friedel-Crafts alkylation or arylation processes, which are well-established in organic synthesis laboratories.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Arzoxifene | 182133-25-1 | C28H29NO4S |
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SB 242084 | 181632-25-7 | C21H21Cl3N4O2 |
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3-Amino-2-(2-fluorophenoxy)pyridine | 175135-66-7 | C11H9FN2O |
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(Z)-Pyriminobac-methyl | 147411-70-9 | C17H19N3O6 |
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| 57422-10-3 | C16H11NO2 |
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6-phenoxy-9H-Purine | 66085-17-4 | C11H8N4O |
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4-(4-Aminophenoxy)picolinic acid | 1012058-77-3 | C12H10N2O3 |
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4-(4-Nitrophenoxy)pyridin-2(1H)-one | 630125-61-0 | C11H8N2O4 |
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N-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(pyridin-3-yloxy)phenyl)-1H-1,2,4-triazol-5-amine | 877874-59-4 | C20H13ClF3N5O |
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Methyl 4-(pyridin-3-yloxy)benzoate | 877874-61-8 | C13H11NO3 |
Related Literature
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Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
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Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
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Tanya Ostapenko,Peter J. Collings,Samuel N. Sprunt,J. T. Gleeson Soft Matter, 2013,9, 9487-9498
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