93706-76-4 Usage
Uses
Used in Coatings Industry:
3-Perfluorooctyl-2-hydroxypropyl methacrylate is used as a component in coatings for its ability to enhance surface properties, such as providing non-stick surfaces and improving chemical and water resistance. This makes it suitable for applications where durability and resistance to environmental factors are required.
Used in Lubricants Industry:
In the lubricants industry, 3-Perfluorooctyl-2-hydroxypropyl methacrylate is used to improve the performance of lubricants by reducing friction and wear, thanks to its low surface tension and hydrophobic nature. This contributes to the longevity and efficiency of machinery and mechanical components.
Used in Medical Devices Industry:
3-Perfluorooctyl-2-hydroxypropyl methacrylate is utilized in the medical devices industry for its biocompatible properties and ability to be modified or crosslinked, making it suitable for use in various medical applications, including implants and diagnostic tools.
Check Digit Verification of cas no
The CAS Registry Mumber 93706-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,0 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93706-76:
(7*9)+(6*3)+(5*7)+(4*0)+(3*6)+(2*7)+(1*6)=154
154 % 10 = 4
So 93706-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H11F17O3/c1-5(2)7(34)35-4-6(33)3-8(16,17)9(18,19)10(20,21)11(22,23)12(24,25)13(26,27)14(28,29)15(30,31)32/h6,33H,1,3-4H2,2H3
93706-76-4Relevant academic research and scientific papers
Cirkva, Vladimir,Ameduri, Bruno,Boutevin, Bernard,Paleta, Oldrich
, p. 53 - 61 (1997)
The reactions of oxiranes RFCH2CH(-O-)CH2 (RF≡C4F9, C6F13, C8F17; 4a-4c) with a series of alkanols in the presence of a Lewis acid took place at the terminal carbon atom with complete regioselectivity. 2-Hydroxyethyl methacrylate and acrylate reacted similarly. The reaction with alkane diols was controlled to proceed with one or two molecules of the oxiranes chemoselectively. Non-regioselective, base-catalysed ring opening by methacrylic acid (83% terminal attack) was discussed on the basis of the hard and soft acids and bases (HSAB) concept. A convenient transformation of the oxiranes to the corresponding diols 13a-13c via dioxolane intermediates, and their conversion to bis-methacrylates, was accomplished with overall yields of 75%-79%. Thiourea converted the oxiranes into the corresponding thiiranes (15a-15c). The reactions afforded products generally in yields of 82%-98%.
