ALLYL 1,1,2,2-TETRAFLUOROETHYL ETHER

  • Name:ALLYL 1,1,2,2-TETRAFLUOROETHYL ETHER
  • CAS:1428-33-7
  • Purity:99%
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  • Molecular Formula:C5H6 F4 O
  • Molecular Weight:158.096
  • Vapor Pressure:107mmHg at 25°C 
  • Refractive Index:1.328 
  • Boiling Point:77.4°Cat760mmHg 
  • Flash Point:°C 
  • PSA:9.23000 
  • Density:1.173g/cm3 
  • LogP:2.04690 

ALLYL 1,1,2,2-TETRAFLUOROETHYL ETHER(Cas 1428-33-7) Usage

General Description

ALLYL 1,1,2,2-TETRAFLUOROETHYL ETHER, also known as allyl perfluorovinyl ether, is a chemical compound with the molecular formula C5H4F8O. It is a colorless, flammable liquid with a faint sweet odor. ALLYL 1,1,2,2-TETRAFLUOROETHYL ETHER is primarily used as a monomer in the production of perfluorocarbon polymers, which have applications in making films, coating, and other industrial products. It is also used as a reactive intermediate in the synthesis of other chemicals and materials. Allyl 1,1,2,2-tetrafluoroethyl ether is known to be highly stable and inert, with low reactivity towards most common chemical reactions. However, it should be handled carefully due to its flammability and potential for hazardous reactions with certain chemicals.

InChI:InChI=1/C5H6F4O/c1-2-3-10-5(8,9)4(6)7/h2,4H,1,3H2

1428-33-7 Relevant articles

Cyclizations of 5-hexenyl, 6-heptenyl, 7-octenyl, and 8-nonenyl radicals. The kinetic and regiochemical impact of fluorine and oxygen substituents

Li, Anrong,Shtarev, Alexander B.,Smart, Bruce E.,Yang, Zhen-Yu,Lusztyk, Janusz,Ingold, Keith U.,Bravo, Anna,Dolbier Jr., William R.

, p. 5993 - 5999 (1999)

Using competition kinetic methodology, r...

Synthesis and Evaluation of Phospholipid Analogues as Inhibitors of Cobra Venom Phospholipase A2

Yuan, Wei,Berman, Richard J.,Gelb, Michael H.

, p. 8071 - 8081 (2007/10/02)

Analogues of phospholipids that contain ...

1428-33-7 Process route

polytetrafluoroethylene
116-14-3,82785-14-6

polytetrafluoroethylene

allyl alcohol
107-18-6

allyl alcohol

1,1,2,2-tetrafluoroethyl allyl ether
1428-33-7

1,1,2,2-tetrafluoroethyl allyl ether

Conditions
Conditions Yield
With sodium; In 1,4-dioxane;
With sodium hydride; In tetrahydrofuran; at -10 - -5 ℃; for 6h;
C<sub>5</sub>H<sub>5</sub>F<sub>4</sub>O

C5H5F4O

1,1,2,2-tetrafluoroethyl allyl ether
1428-33-7

1,1,2,2-tetrafluoroethyl allyl ether

3-methyl-4,4,5,5-tetrafluoro-1-oxacyclopentane
240140-63-0

3-methyl-4,4,5,5-tetrafluoro-1-oxacyclopentane

Conditions
Conditions Yield
With tris-(trimethylsilyl)silane; In benzene-d6; at 25 ℃; Kinetics; Photolysis;

1428-33-7 Upstream products

  • 116-14-3
    116-14-3

    polytetrafluoroethylene

  • 107-18-6
    107-18-6

    allyl alcohol

1428-33-7 Downstream products

  • 756-76-3
    756-76-3

    trichloro-[3-(1,1,2,2-tetrafluoro-ethoxy)-propyl]-silane

  • 1554-54-7
    1554-54-7

    Chlor-methyl-<3-(1.1.2.2-tetrafluor-aethoxy)-propyl>-phenyl-silan

  • 1512-95-4
    1512-95-4

    Dichlor-<3-(1.1.2.2-tetrafluor-ethoxy)-propyl>-<4-fluor-phenyl>-silan

  • 731-21-5
    731-21-5

    Dichlor-<3-(1.1.2.2-tetrafluor-ethoxy)-propyl>-phenyl-silan