3832-65-3 Usage
Uses
Used in Lubricant Additives:
1,4-Bis(1,1,2,2-tetrafluoroethoxy)benzene is used as a lubricant additive to enhance the performance and longevity of lubricants. Its heat and chemical resistance contribute to the improved stability and efficiency of the lubricants in various mechanical systems.
Used in Polymer and Plastics Production:
1,4-Bis(1,1,2,2-tetrafluoroethoxy)benzene is utilized in the production of polymers and plastics due to its stability and resistance to heat and chemicals. Its incorporation into these materials can lead to enhanced durability and performance in a variety of end products.
Used in Industrial Applications:
1,4-Bis(1,1,2,2-tetrafluoroethoxy)benzene is employed across various industries for its ability to improve the properties of materials and products. Its low toxicity and non-harmful effects on human health and the environment when used as intended make it a suitable choice for a wide range of applications. However, it is important to follow proper handling and storage procedures to minimize potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 3832-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3832-65:
(6*3)+(5*8)+(4*3)+(3*2)+(2*6)+(1*5)=93
93 % 10 = 3
So 3832-65-3 is a valid CAS Registry Number.
3832-65-3Relevant academic research and scientific papers
Fluorinated arylethers and methods for use thereof
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Page/Page column 4, (2008/06/13)
The invention provides new fluorinated solvents that have many uses. One such use is as a solvent useful in the deposition of organic active materials in the manufacture of organic electronic devices. The new fluorinated solvents are fluorinated arylethers and can be readily prepared from corresponding phenols and fluorinated olefins.
Tandem Nucleophilic Additions of Aryloxides
Arnold-Stanton, Regina,Lemal, David M.
, p. 151 - 157 (2007/10/02)
Hydroquinone disodium salt added sequentially to tetrafluoroethylene and carbon dioxide to yield a symmetrical dicarboxylic acid, which was transformed into the corresponding dimethyl ester, diol, diamide, and diamine.Chlorotrifluoroethylene in analogous reactions gave the corresponding diester and diol in excellent yield.When this kind of transformation was attempted on phloroglucinol, the Kolbe-Schmitt carboxylation reaction intervened.Despite serious competition from addition/elimination processes under typical reaction conditions, the tandem addition of phenoxide ion to hexafluoropropene and carbon dioxide was carried out successfully at lower temperatures and higher carbon dioxide pressures.
