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2,2,2-TRIFLUOROETHYL TRIFLUOROACETATE CAS:407-38-5

2,2,2-Trifluoroethyl trifluoroacetate (TFETA) is a notable chemical compound recognized for its unique molecular structure and versatile applications in various industrial sectors. With the chemical formula C4H3F6O2, TFETA is characterized by the presence of both trifluoroethyl and trifluoroacetate moieties. This compound is synthesized through esterification of trifluoroacetic acid with 2,2,2-trifluoroethanol, resulting in a colorless liquid with a high boiling point and remarkable chemical stability. TFETA is valued for its role as a fluorinated building block in organic synthesis, particularly in the production of specialty chemicals, pharmaceutical intermediates, and materials requiring enhanced chemical resistance and stability.


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Application and Effect:

2,2,2-Trifluoroethyl trifluoroacetate (TFETA) is a versatile compound with distinctive chemical properties that contribute to its broad utility in various industrial applications. Properties TFETA is characterized by its molecular structure, featuring a trifluoroethyl group (-CF3CH2-) attached to a trifluoroacetate ester (-OC(O)CF3). This combination results in a clear, colorless liquid with a high boiling point, around 145°C, and excellent solubility in organic solvents. The compound exhibits low reactivity due to the electron-withdrawing nature of fluorine atoms, imparting robust chemical stability under a wide range of conditions. TFETA's properties make it suitable for applications requiring inertness, such as in the synthesis of stable intermediates and protective coatings. Uses Organic Synthesis: TFETA serves as a crucial intermediate in organic synthesis, where it participates in reactions to introduce fluorinated functionalities into complex molecules. This capability is particularly valuable in pharmaceutical chemistry for creating fluorinated drugs and in the production of specialty chemicals where enhanced stability and chemical resistance are desired. Materials Science: The chemical stability and solubility of TFETA make it an ideal component in the formulation of coatings and materials with specific performance requirements. It is utilized to enhance the durability and protective properties of surfaces against environmental degradation and chemical attack, contributing to the longevity of materials in applications ranging from automotive coatings to electronic components. Pharmaceutical Applications: TFETA's role in organic synthesis extends to pharmaceutical applications, where its fluorinated structure can modulate biological activity and pharmacokinetic properties of drug molecules. This makes it a valuable tool in drug discovery and development processes aimed at improving therapeutic efficacy and bioavailability. Synthesis TFETA is synthesized through the esterification of trifluoroacetic acid (CF3COOH) with 2,2,2-trifluoroethanol (CF3CH2OH) under acidic conditions. The reaction produces TFETA along with water as a byproduct, which can be purified via distillation or solvent extraction to achieve high purity suitable for industrial applications. The straightforward synthesis and handling of TFETA contribute to its cost-effectiveness and widespread use across various sectors requiring fluorinated compounds. In summary, 2,2,2-trifluoroethyl trifluoroacetate is a versatile compound essential in organic synthesis, materials science, and pharmaceutical chemistry. Its unique chemical properties enable the development of advanced materials and pharmaceuticals with enhanced stability and performance characteristics, underscoring its significance in modern industrial applications.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C4H2F6O2
Assay 99%
Appearance white powder
CAS No.  407-38-5
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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