42145-66-4 Usage
Uses
Used in Chemical Synthesis:
2-(1,1,2,2-Tetrafluoroethoxy)toluene is used as an intermediate in the synthesis of other organic compounds, contributing to the creation of a wide range of chemical products due to its reactive nature.
Used in Polymer and Resin Manufacturing:
2-(1,1,2,2-TETRAFLUOROETHOXY)TOLUENE is utilized in the production of polymers and resins, where its unique properties enhance the performance characteristics of the final products, such as their stability and resistance to certain conditions.
Used as a Solvent:
2-(1,1,2,2-Tetrafluoroethoxy)toluene also serves as a solvent in various industrial processes, leveraging its ability to dissolve other substances, which is crucial for certain manufacturing techniques and chemical reactions.
Used in Industrial Product Manufacturing:
Its application extends to the manufacturing of other industrial products, where it is employed for its specific chemical properties that improve the quality or performance of the end products.
Safety Considerations:
Check Digit Verification of cas no
The CAS Registry Mumber 42145-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,4 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42145-66:
(7*4)+(6*2)+(5*1)+(4*4)+(3*5)+(2*6)+(1*6)=94
94 % 10 = 4
So 42145-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8F4O/c1-6-4-2-3-5-7(6)14-9(12,13)8(10)11/h2-5,8H,1H3
42145-66-4Relevant articles and documents
A practical synthesis of aryl tetrafluoroethyl ethers via the improved reaction of phenols with 1,2-dibromotetrafluoroethane
Li, Jianqing,Qiao, Jennifer X.,Smith, Daniel,Chen, Bang-Chi,Salvati, Mark E.,Roberge, Jacques Y.,Balasubramanian, Balu N.
, p. 7516 - 7519 (2008/03/14)
An efficient and practical synthesis of various aryl tetrafluoroethyl ethers by the reaction of phenols with 1,2-dibromotetrafluoroethane and the subsequent reduction with zinc dust was described. The nucleophilic substitution of 1,2-dibromotetrafluoroethane with phenols initiated by bromophilic attack was improved by using Cs2CO3 as a base and DMSO as a solvent.