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Ethylene glycol bis(1,1,2,2-tetrafluoroethyl) ether, also known as "Bis(2,2,2-trifluoroethyl) ether", is an organic chemical compound with the molecular formula C6H8F8O2. It belongs to the category of ethers, characterized by an ether group an oxygen atom connected to two alkyl or aryl groups. Ethylene glycol bis(1,1,2,2-tetrafluoroethyl) ether features the 1,3-dioxolan substructure and is known for its excellent stability and solvent properties.

358-39-4

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358-39-4 Usage

Uses

Used in Chemical Synthesis:
Ethylene glycol bis(1,1,2,2-tetrafluoroethyl) ether is used as a solvent in various chemical synthesis processes for its ability to dissolve a wide range of compounds and facilitate reactions.
Used in Industrial Applications:
In the industrial sector, Ethylene glycol bis(1,1,2,2-tetrafluoroethyl) ether is utilized as a component in the production of certain materials, taking advantage of its stability and solvent characteristics to ensure the quality and performance of the final products.

Check Digit Verification of cas no

The CAS Registry Mumber 358-39-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 358-39:
(5*3)+(4*5)+(3*8)+(2*3)+(1*9)=74
74 % 10 = 4
So 358-39-4 is a valid CAS Registry Number.

358-39-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2-tetrafluoro-1-[2-(1,1,2,2-tetrafluoroethoxy)ethoxy]ethane

1.2 Other means of identification

Product number -
Other names Ethane,1,2-bis(1,1,2,2-tetrafluoroethoxy)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:358-39-4 SDS

358-39-4Downstream Products

358-39-4Relevant academic research and scientific papers

Preparation method of fluoroether

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Paragraph 0039; 0040, (2021/07/09)

The invention discloses a preparation method of fluoroether. The method comprises the following steps: reacting ester with fluoroolefin in a solvent under the action of a catalyst, and filtering and rectifying the obtained reaction liquid to obtain a fluoroether product. The method has the advantages of being simple in process, economical, efficient, green and environmentally friendly.

SYNTHESIS OF PERFLUORINATED ETHERS BY AN IMPROVED SOLUTION PHASE DIRECT FLUORINATION PROCESS

Sievert, Allen C.,Tong, Walter R.,Nappa, Mario J.

, p. 397 - 418 (2007/10/02)

We have developed schemes to make perfluorinated ethers that cover a wide range of molecular weights and boiling points.We describe a relationship that can be used to predict the boiling points of perfluoro polyethers; this is used to assist in the combination of reagents for synthesizing a target having particular physical properties such as boiling point, etc.Our first scheme is to build molecular weight by condensing polyols with fluoro-olefins such as TFE and TFP.These intermediates are then fluorinated by a simple solution phase, batch, photo-assisted directfluorination to give high yields of isomerically pure perfluorinated ethers.In a second scheme we use ethylene oxide to fine-tune the molecular weight of the polyol, and the weight of these can be extended by reaction with an appropriate fluoro-olefin.These intermediates can be fluorinated using uor batch fluorinator to make new perfluorinated ethers of a specific molecular weight and boiling point.

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