Hot Sale Buy Reliable Quality 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl methacrylate/2-(Perfluorohexyl)ethyl methacrylate 2144-53-8 Cheap Price
- Molecular Formula:C12H9F13O2
- Molecular Weight:432.181
- Vapor Pressure:0.116mmHg at 25°C
- Refractive Index:n20/D 1.346(lit.)
- Boiling Point:220 °C at 760 mmHg
- Flash Point:84.6 °C
- PSA：26.30000
- Density:1.459g/cm3
- LogP:5.23460
2-(Perfluorohexyl)ethyl methacrylate(Cas 2144-53-8) Usage
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Uses
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Surface structure and outer group orientation in poly(perfluoroalkylethyl methacrylate) consist of Tridecafluorohexylethyl Methacrylate.Semifluorinated diblock copolymers based on Me methacrylate and Tridecafluorohexylethyl Methacrylate were prepared by nucleophilic catalyzed group transfer polymerization. |
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Flammability and Explosibility
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Nonflammable |
InChI:InChI=1/C12H9F13O2/c1-5(2)6(26)27-4-3-7(13,14)8(15,16)9(17,18)10(19,20)11(21,22)12(23,24)25/h1,3-4H2,2H3
2144-53-8 Relevant articles
Synthesis of fluorinated block copolymers and their application as novel polymerisation surfactants in supercritical carbon dioxide
Yong, Tuck-Mun,Hems, William P.,Van Nunen, Johanna L. M.,Holmes, Andrew B.,Steinke, Joachim H. G.,Taylor, Philip L.,Segal, John A.,Griffin, David A.
, p. 1811 - 1812 (1997)
Screened anionic copolymerisation of met...
METHOD FOR PRODUCING FLUORINE-CONTAINING (METH) ACRYLATE
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Paragraph 0043-0047; 0059, (2021/03/13)
To provide a method for producing fluori...
Dehydrogenative Silylation of Alkenes for the Synthesis of Substituted Allylsilanes by Photoredox, Hydrogen-Atom Transfer, and Cobalt Catalysis
Yu, Wan-Lei,Luo, Yong-Chun,Yan, Lei,Liu, Dan,Wang, Zhu-Yin,Xu, Peng-Fei
supporting information, p. 10941 - 10945 (2019/07/17)
A synergistic catalytic method combining...
Cyanide-Free One-Pot Synthesis of Methacrylic Esters from Acetone
Koyama, Minoru,Kawakami, Takafumi,Okazoe, Takashi,Nozaki, Kyoko
, p. 10913 - 10917 (2019/08/02)
Methacrylic esters, represented by methy...
METHOD FOR PRODUCING UNSATURATED ACID AND/OR UNSATURATED ACID ESTER
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Paragraph 0110-0111, (2015/07/02)
The present invention relates to a metho...
2144-53-8 Process route
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2043-57-4,71215-70-8
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane
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6900-35-2
potassium methacrylate
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647-42-7
1H,1H,2H,2H-tridecafluoro-n-octanol
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25291-17-2
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene
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2144-53-8
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-methylpropenoate
Conditions
| Conditions |
Yield |
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With
10H-phenothiazine;
In
tert-butyl alcohol;
at 130 - 170 ℃;
for 6 - 9h;
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2043-57-4,71215-70-8
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane
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-
6900-35-2
potassium methacrylate
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25291-17-2
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene
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-
2144-53-8
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-methylpropenoate
Conditions
| Conditions |
Yield |
|
With
10H-phenothiazine;
In
tert-butyl alcohol;
at 160 ℃;
for 9h;
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2144-53-8 Upstream products
