2261-99-6 Usage
General Description
1H,1H,7H-Dodecafluoroheptyl methacrylate is a chemical compound with the formula C13H17F13O2. It is a fluorinated methacrylate that is commonly used in the production of polymers and coatings due to its water and oil repellent properties. It is a clear, colorless liquid with a characteristic odor and is highly flammable. 1H,1H,7H-Dodecafluoroheptyl methacrylate is known for its low surface energy and high chemical stability, making it a valuable ingredient in the manufacturing of products such as non-stick coatings, water-repellent fabrics, and oil-resistant materials. Due to its highly fluorinated structure, it is also considered to be environmentally persistent and bioaccumulative, raising concerns about its potential impact on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 2261-99-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2261-99:
(6*2)+(5*2)+(4*6)+(3*1)+(2*9)+(1*9)=76
76 % 10 = 6
So 2261-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H8F12O2/c1-4(2)5(24)25-3-7(14,15)9(18,19)11(22,23)10(20,21)8(16,17)6(12)13/h6H,1,3H2,2H3
2261-99-6Relevant articles and documents
Polyfluoroalkyl chlorosulfites as new polyfluorinating agents
Rakhimov,Vostrikova
, p. 1162 - 1165 (2002)
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.
