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Tetrafluorosuccinic anhydride, with the chemical formula C4F4O3, is an organic compound that features four fluorine atoms attached to a succinic anhydride backbone. It is known for its unique chemical properties, including its reactivity and stability, which make it a versatile building block in various chemical reactions and applications.

699-30-9

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699-30-9 Usage

Uses

Used in Energy Storage Industry:
Tetrafluorosuccinic anhydride is used as a key component in the development of advanced materials for energy storage devices, specifically to enhance the performance of batteries. Its incorporation into battery materials can lead to improved energy density, cycle life, and overall efficiency, making it a valuable asset in the advancement of energy storage technologies.
Used in Chemical Synthesis:
In the chemical synthesis industry, tetrafluorosuccinic anhydride serves as a versatile intermediate for the production of a wide range of fluorinated compounds. Its reactivity and stability make it an ideal candidate for the synthesis of pharmaceuticals, agrochemicals, and specialty materials that require fluorine-containing moieties for enhanced properties.
Used in Material Science:
Tetrafluorosuccinic anhydride is also utilized in the development of novel materials with unique properties, such as high thermal stability, chemical resistance, and low surface energy. These materials can find applications in various industries, including aerospace, automotive, and electronics, where such properties are highly desirable.

Check Digit Verification of cas no

The CAS Registry Mumber 699-30-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 699-30:
(5*6)+(4*9)+(3*9)+(2*3)+(1*0)=99
99 % 10 = 9
So 699-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C4F4O3/c5-3(6)1(9)11-2(10)4(3,7)8

699-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrafluorosuccinic Anhydride

1.2 Other means of identification

Product number -
Other names 3,3,4,4-tetrafluorooxolane-2,5-dione

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:699-30-9 SDS

699-30-9Relevant academic research and scientific papers

Preparation method of fluorine-containing carboxylic acid

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Paragraph 0033-0034; 0036, (2020/07/12)

The invention discloses a preparation method of fluorine-containing carboxylic acid. The method comprises the following steps: reacting fluorine-containing carboxylate used as a raw material with an acylating chlorination reagent to obtain a corresponding mixture of fluorine-containing acyl chloride and fluorine-containing anhydride, and hydrolyzing and drying the mixture of fluorine-containing acyl chloride and fluorine-containing anhydride to obtain high-purity fluorine-containing carboxylic acid. The method provided by the invention is suitable for post-treatment of fluorine-containing carboxylic acid prepared by a fluorine-containing olefin (monoolefine, diene, cycloolefin and the like) oxidation method, replaces the traditional strong acid acidification and ether continuous extractionprocess, and is simpler, more convenient and more applicable; and the method can also be used for recovering and purifying a fluorine-containing carboxylate emulsifier. The purity of the fluorine-containing carboxylic acid prepared by the method can reach 98% or above.

Some fluorinated heterocyclic and acyclic derivatives of chlorocarbonylsulfenyl chloride

John, Earnest Obed,Shreeve, Jean'ne M.

, p. 429 - 438 (2007/10/02)

For the first time, fluorinated oxathialones, polyfluoroalkylchlorothioformates, chlorocarbonylpolyfluoroalkylsulfenate esters, a chlorocarbonylhexafluoroisopropylidenimino sulfenate, and a 5-tri-fluoromethyl-2-oxo-1,3,4-oxathiazole were synthesized by reacting chlorocarbonylsulfenyl chloride with RfC(O)CH2C(O)R′ (Rf = CF3; R'= CF3, OC2H5), RfO-Li+ (Rf = CF3CH2, (CF3)2C=N-Li+ and CF3C(O)NH2. Perfluorosuccinic acid and mercury(II) trifluoroacetate with ClC(O)SCI gave their respective anhydrides.

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