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2-Trifluoromethyl thioxanthone CAS:1693-28-3

2-Trifluoromethyl thioxanthone is a specialized aromatic compound that combines a thioxanthone structure with a trifluoromethyl (-CF3) substituent at the 2-position. This unique configuration imparts notable physicochemical properties, making it valuable in various applications, particularly in organic electronics and photoinitiators for polymerization processes. The trifluoromethyl group enhances the stability and electron affinity of the compound, increasing its efficacy in photochemical reactions. Understanding its profile is crucial for researchers engaged in the development of advanced materials and technologies in molecular and polymer sciences.


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Application and Effect:

2-Trifluoromethyl thioxanthone (C15H9F3OS) is an interesting derivative of thioxanthone, characterized by the presence of a trifluoromethyl (-CF3) group at the 2-position of the aromatic system. The thioxanthone core consists of a fused benzothiophene structure featuring a carbonyl group, which is an essential motif in organic photochemistry. The incorporation of the trifluoromethyl group significantly alters the compound's physical and chemical properties, making it suitable for diverse applications, particularly in the fields of organic electronics, photoinitiators, and dye-sensitized solar cells. The trifluoromethyl substituent not only imparts hydrophobic character but also enhances the electronic properties of 2-trifluoromethyl thioxanthone. This modification leads to increased thermal stability, elevated electron-withdrawing capabilities, and an extended absorption spectrum, which are advantageous for light-harvesting applications. As a result, this compound can efficiently participate in photochemical reactions, generating reactive species upon exposure to UV light, thus serving as an effective photoinitiator in polymerization processes. In addition to its role in photoinduced polymerization, 2-trifluoromethyl thioxanthone is also explored for its potential applications in organic light-emitting diodes (OLEDs) and flexible electronics. Its ability to modify the electronic and optical properties of the light-emitting materials can lead to the development of devices with enhanced performance metrics. Furthermore, studies of 2-trifluoromethyl thioxanthone contribute to understanding the behavior of fluorinated compounds in various chemical environments, paving the way for innovations in materials science and molecular engineering. In summary, the unique properties of 2-trifluoromethyl thioxanthone make it a valuable compound for advancing research and applications in organic photochemistry and material development, reflecting its growing significance in modern chemistry.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C14H7F3OS
Assay 99%
Appearance white powder
CAS No.  1693-28-3
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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