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2,3,3,3-tetrafluoro-2-(pentafluoroethoxy)propanoyl fluoride is a colorless, odorless liquid chemical compound with the molecular formula C5F13O3F4. It is known for its high reactivity, stability, and low toxicity, making it a valuable intermediate in the production of fluorochemicals and pharmaceuticals. Its strong fluorinating and acylating properties contribute to its wide application in the manufacturing of specialty chemicals and high-performance materials.

1682-78-6

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1682-78-6 Usage

Uses

Used in Fluorochemical Production:
2,3,3,3-tetrafluoro-2-(pentafluoroethoxy)propanoyl fluoride is used as an intermediate for the synthesis of various fluorochemicals. Its high reactivity and stability make it an essential component in the production of these specialty chemicals.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2,3,3,3-tetrafluoro-2-(pentafluoroethoxy)propanoyl fluoride serves as a key intermediate in the synthesis of certain drugs. Its unique properties allow for the creation of novel pharmaceutical compounds with potential therapeutic benefits.
Used in Organic Synthesis as a Reagent:
Due to its strong fluorinating and acylating properties, 2,3,3,3-tetrafluoro-2-(pentafluoroethoxy)propanoyl fluoride is commonly used as a reagent in organic synthesis. It aids in the formation of new chemical bonds and the synthesis of complex organic molecules.
Used in High-Performance Material Manufacturing:
2,3,3,3-tetrafluoro-2-(pentafluoroethoxy)propanoyl fluoride is utilized in the production of high-performance materials, such as polymers and coatings, that exhibit exceptional properties like heat resistance, chemical resistance, and low surface energy. Its incorporation into these materials enhances their performance and durability in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1682-78-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1682-78:
(6*1)+(5*6)+(4*8)+(3*2)+(2*7)+(1*8)=96
96 % 10 = 6
So 1682-78-6 is a valid CAS Registry Number.

1682-78-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,3,3-tetrafluoro-2-(1,1,2,2,2-pentafluoroethoxy)propanoyl fluoride

1.2 Other means of identification

Product number -
Other names 2,3,3,3-tetrafluoro-2-(pentafluoroethoxy)propionic acid fluoride

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:1682-78-6 SDS

1682-78-6Downstream Products

1682-78-6Relevant academic research and scientific papers

METHOD FOR PREPARING FLUORINE-CONTAINING VINYL ETHER

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Paragraph 0030-0031, (2014/10/29)

Provided is a method for preparing fluorine-containing vinyl ether. The method comprises: carrying out hydrolytic neutralization on a small molecular weight byproduct which is produced in the process of preparing perfluoropolyether or a perfluorinated surfactant by photooxidation of fluorine-containing olefin; and obtaining fluorine-containing vinyl ether by drying and cracking. The byproduct produced in the process of preparing perfluoropolyether or the perfluorinated surfactant is utilized, thereby solving the emission problem of industrial wastes, reducing environment pollution, and generating available fluorine-containing vinyl ether.

A new procedure for preparing perfluoroalkoxypropanoic acid fluorides

Igumnov,Lekontseva,Shipigusev,Mukhametshin

, p. 435 - 437 (2008/02/01)

Condensation of perfluoro carboxylic acid fluorides with hexafluoropropene epoxide in the presence of N,N, N,N-tetraalkyldiaminomethanes was studied.

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