2356-61-8 Usage
Uses
Used in Refrigeration Industry:
Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether is used as a refrigerant for its non-flammable and stable properties, making it a safer alternative to traditional refrigerants.
Used in Industrial Solvents:
In the chemical industry, Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether serves as a solvent due to its ability to dissolve a wide range of substances and its compatibility with various materials.
Used in Chemical Synthesis:
Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether is also utilized in chemical synthesis processes, taking advantage of its stability and reactivity under controlled conditions to produce desired products.
Used in Specialty Fluids:
Due to its unique properties, Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether is employed in the formulation of specialty fluids for specific applications where its non-flammability and stability are critical.
Used in Heat Transfer Applications:
Its thermal properties make Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether suitable for use in heat transfer systems where a non-flammable and stable fluid is required.
Used in Electronics Cleaning:
In the electronics industry, Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether is used for cleaning delicate components due to its ability to effectively remove contaminants without causing damage to sensitive materials.
Used in Environmentally Friendly Applications:
Trifluoromethyl 1,1,2,2-tetrafluoroethyl ether is considered an environmentally friendly option for various applications due to its low toxicity and non-flammable nature, reducing the environmental impact compared to other chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 2356-61-8 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 2356-61:
(6*2)+(5*3)+(4*5)+(3*6)+(2*6)+(1*1)=78
78 % 10 = 8
So 2356-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C3HF7O/c4-1(5)2(6,7)11-3(8,9)10/h1H
2356-61-8Relevant 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.
THERMOGRAPHIC INVESTIGATION OF THE DECARBOXYLATION OF SALTS OF PERFLUORINATED CARBOXYLIC ACIDS
Gubanov, V. A.,Zevakin, I. A.,Gurari, V. E.,Tumanova, A. V.,Dolgopol'skii, I. M.,et al.
, p. 1409 - 1412 (2007/10/02)
The thermal stability of the salts of metals of the first group with perfluorinated carboxylic acids was investigated by a differential thermal method.The calculations of the A, E, and n parameters were made on a Minsk 32 computer.For the investigated series of salts the reactions has first-order kinetics.In the case of the pyrolysis of the salts of perfluoromethoxypropionic acid the yield of perfluoromethyl vinyl ether depends not only on the cation of the salt but is determined to a significant degree by the structural features of the carbon skeleton.Tetrafluoroethylene and perfluoromethoxypropionyl fluoride were detected as side products.A mechanism for the process, which explains the formation of the main reaction products, was proposed and confirmed experimentally.
