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BIS[2-(FLUOROSULFONYL)TETRAFLUOROETHYL]ETHER is a synthetic chemical compound characterized by a complex molecular structure. It is likely to possess properties common to fluorochemicals, which are known for their stability, electric insulating properties, and resistance to heat and chemical reactions. These attributes make fluorochemicals versatile and valuable in a range of applications across different industries.

146829-79-0

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146829-79-0 Usage

Uses

Used in Surfactant Industry:
BIS[2-(FLUOROSULFONYL)TETRAFLUOROETHYL]ETHER is used as a surfactant for its ability to reduce surface tension between liquids and solids, facilitating the mixing and interaction of substances. Its stability and resistance to chemical reactions make it a reliable component in various formulations.
Used in Refrigerant Industry:
In the refrigerant industry, BIS[2-(FLUOROSULFONYL)TETRAFLUOROETHYL]ETHER is used as a component in refrigerant blends, taking advantage of its heat resistance and electric insulating properties to enhance the performance and safety of refrigeration systems.
Used in Medical Imaging:
BIS[2-(FLUOROSULFONYL)TETRAFLUOROETHYL]ETHER is used as a contrast agent in medical imaging, particularly in fluoroscopic procedures. Its chemical properties allow for clear visualization of internal structures without interfering with the imaging process.
Used in Pharmaceuticals:
BIS[2-(FLUOROSULFONYL)TETRAFLUOROETHYL]ETHER is used as an intermediate in the synthesis of pharmaceutical compounds, leveraging its stability and reactivity to produce drugs with desired therapeutic effects.
However, it is important to note that the chemical stability of BIS[2-(FLUOROSULFONYL)TETRAFLUOROETHYL]ETHER, like other fluorochemicals, also raises environmental concerns. Their resistance to degradation can lead to accumulation in the environment, potentially causing long-term ecological impacts. As a result, the use and disposal of such compounds must be carefully managed to mitigate these risks.

Check Digit Verification of cas no

The CAS Registry Mumber 146829-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,8,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 146829-79:
(8*1)+(7*4)+(6*6)+(5*8)+(4*2)+(3*9)+(2*7)+(1*9)=170
170 % 10 = 0
So 146829-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C4F10O5S2/c5-1(6,3(9,10)20(13,15)16)19-2(7,8)4(11,12)21(14,17)18

146829-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-2-fluorosulfonylethoxy)ethanesulfonyl fluoride

1.2 Other means of identification

Product number -
Other names PC2855

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:146829-79-0 SDS

146829-79-0Downstream Products

146829-79-0Relevant articles and documents

A useful synthesis of ω-iodoperfluoroalkanesulfonyl fluorides and perfluoroalkane-α,ω-bis-sulfonyl fluorides

Qiu, Weiming,Burton, Donald J.

, p. 93 - 100 (1993)

ω-Iodoperfluoroalkanesulfonyl fluorides and perfluoroalkane-α,ω-bis-sulfonyl fluorides have been prepared via deiodosulfination, chlorination, and then chlorine-fluorine exchange reaction of α,ω-diiodoperfluoroalkanes I(CF2)nI (n=3, 4, 6).Similar reaction of I(CF2)2O(CF2)2SO2F affords FSO2(CF2)2O(CF2)2SO2F.

Bis(diaryliodonium) perfluorosulfonimide zwitterions as potential photo acid generators

Mei, Hua,Desmarteau, Darryl D.

, p. 12 - 15 (2014/03/21)

Three examples of bis(diaryliodonium) perfluorosulfonimide (BDI-PFSI) zwitterions have been prepared as a potential new class of ionic photo-acid generators for chemically amplified photoresist formulations.

Photoactive Compounds

-

, (2008/12/05)

The present application relates to a compound of formula Ai Xi Bi where Ai and Bi are each individually an organic onium cation; and Xi is anion of the formula ?O3S—CF2CF2OCF2CF2—SO3?. The compounds are useful as photoactive materials.

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