7383-71-3 Usage
Uses
Used in Polymer Production:
2,2,3,3-Tetrafluoropropyl Acrylate is used as a monomer for the synthesis of polymers, leveraging its high thermal stability and resistance to chemicals, oil, and weathering. These properties are particularly beneficial in the creation of materials that require durability and resilience in harsh environments.
Used in Coatings Industry:
In the coatings industry, 2,2,3,3-Tetrafluoropropyl Acrylate is used as a component in the formulation of high-performance coatings. Its chemical resistance and weathering properties contribute to the development of coatings that offer long-lasting protection and durability for various surfaces.
Used in Adhesives Industry:
2,2,3,3-Tetrafluoropropyl Acrylate is used as a component in adhesive formulations, providing enhanced bonding strength and resistance to environmental factors such as heat, chemicals, and moisture. This makes it suitable for applications where strong and durable adhesives are required.
Safety Precautions:
While 2,2,3,3-Tetrafluoropropyl Acrylate offers numerous benefits, it is essential to follow safety handling precautions due to potential hazards such as skin and eye irritation or inhalation. Manufacturers and users should adhere to recommended safety guidelines to minimize risks associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 7383-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7383-71:
(6*7)+(5*3)+(4*8)+(3*3)+(2*7)+(1*1)=113
113 % 10 = 3
So 7383-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H6F4O2/c1-2-4(11)12-3-6(9,10)5(7)8/h2,5H,1,3H2
7383-71-3Relevant academic research and scientific papers
Polyfluoroalkyl chlorosulfites as new polyfluorinating agents
Rakhimov,Vostrikova
, p. 1162 - 1165 (2007/10/03)
The interaction of polyfluorinated alcohols with triethylamine and the kinetics of the reaction of the resulting triethylamine complexes with thionyl chloride were studied, the mechanism of formation of polyfluoroalkyl chlorosulfites was considered, and the optimal reaction conditions were found. The alkylating power of polyfluoroalkyl chlorosulfites was studied in reactions with alkali metal halides (to obtain polyfluorohaloalkanes), in synthesis of acrylic and methacrylic acid esters, and in synthesis of polyfluoroalkyl ethers (with polyfluoroalkyl 1-adamantyl ethers as example).
SYNTHESIS AND PHYSICOCHEMICAL PROPERTIES OF ORGANOFLUORINE ESTERS OF ACRYLIC, METHACRYLIC, AND MALEIC ACIDS.
Gol'din,Averbakh,Nekrasova,Lavygin,Leitan,Chalbysheva
, p. 1244 - 1247 (2007/10/02)
The purpose of this work is to synthesize, and to study the physicochemical properties of organofluorine acrylates, methacrylates, and maleates.
