2356-62-9 Usage
Uses
Used in Medical Anesthesia:
1,2,2,2-Tetrafluoroethyl trifluoromethyl ether is used as an inhalation anesthetic in the medical field. Its properties, such as being nonflammable and having a high boiling point, make it a robust and reliable choice for surgical procedures. It is particularly valued for its rapid onset and offset of action, which allows for precise control during anesthesia.
Used in Research Applications:
Due to its unique properties, 1,2,2,2-tetrafluoroethyl trifluoromethyl ether is also used in research settings. Scientists are exploring its potential applications in various fields, including pharmaceutical development and material science, where its chemical stability and high fluorine content may offer novel opportunities for innovation.
Used in Pharmaceutical Development:
1,2,2,2-Tetrafluoroethyl trifluoromethyl ether is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its chemical properties, such as stability and reactivity, make it a valuable component in the development of new drugs and therapeutic agents.
Used in Material Science:
In the field of material science, 1,2,2,2-tetrafluoroethyl trifluoromethyl ether is used for the development of new materials with specific properties. Its high fluorine content and chemical stability contribute to the creation of materials with unique characteristics, such as enhanced durability, heat resistance, or chemical resistance.
Safety Considerations:
Check Digit Verification of cas no
The CAS Registry Mumber 2356-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2356-62:
(6*2)+(5*3)+(4*5)+(3*6)+(2*6)+(1*2)=79
79 % 10 = 9
So 2356-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C3HF7O/c4-1(2(5,6)7)11-3(8,9)10/h1H
2356-62-9Relevant academic research and scientific papers
Relative Rate Constants for the Reactions of CF3OF with Olefins in Solution
Navarrini, W.,Russo, A.,Tortelli, V.
, p. 6441 - 6443 (2007/10/03)
The addition reactions of CF3OF to chloro fluoro olefins have been studied in solution at low temperature (-78, -105 deg C), and their relative rate constants have been determined using the kinetic approach of competition reactions.The reactivity and regio- and stereoselectivity are consistent with a free radical chain-propagating reaction in which the alkenes are attacked by the CF3O* radical generated by homolytic cleavage of the O-F bond in the CF3OF molecule.
Synthesis of Perfluoroethylmethylether by Direct Fluorination
Sekiya, Akira,Ueda, Kunimasa
, p. 609 - 612 (2007/10/02)
The direct fluorination of trifluoromethylethers prepared from ethylene or fluorinated ethylenes with trifluoromethyl hypofluorite proceeded in excellent yield to obtain perfluoroethylmethylethers.
