Chloromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether

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Chloromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether

  • Name Chloromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether
  • CAS 26103-07-1
  • Purity 99%
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Product Details

Chloromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether GMP Manufacturer Global Trade 26103-07-1 with Fast Delivery

  • Molecular Formula: C4H3ClF6O
  • Molecular Weight: 216.511
  • Vapor Pressure: 52.835mmHg at 25°C 
  • Refractive Index: 1.31 
  • Boiling Point: 94.979 °C at 760 mmHg 
  • Flash Point: 11.244 °C 
  • PSA: 9.23000 
  • Density: 1.488 g/cm3 
  • LogP: 2.69250 

Chloromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether(Cas 26103-07-1) Usage

General Description

Chloromethyl-1,1,1,3,3,3-hexafluoroisopropyl ether is a chemical compound that is often used as a solvent and reagent in various chemical reactions and processes. It is a fluorinated ether compound, containing carbon, hydrogen, chlorine, and fluorine atoms. This chemical is characterized by its highly fluorinated structure, which provides it with unique chemical and physical properties. It is commonly used as a solvent in organic synthesis, as well as in the production of various industrial chemicals and pharmaceuticals. Additionally, it can also be used as a reagent in the preparation of certain organic compounds, making it a valuable tool in organic chemistry research and development. However, it is important to handle and use this compound with caution, as it may pose risks to human health and the environment if not handled properly.

InChI:InChI=1/C4H3ClF6O/c5-1-12-2(3(6,7)8)4(9,10)11/h2H,1H2

26103-07-1 Relevant articles

An efficient and environmentally friendly synthesis of the inhalation anesthetic sevoflurane

Bieniarz, Christopher,Behme, Chris,Ramakrishna, Kornepati

, p. 99 - 102 (2000)

We report a new, high yield, single vess...

A safe and efficient process for the synthesis of the inhalation anesthetic sevoflurane

Ramakrishna, Kornpati,Behme, Chris,Schure, Ralph M.,Bieniarz, Christopher

, p. 581 - 584 (2000)

A novel method for the synthesis of 1,1,...

Method for synthesizing sevoflurane intermediate

-

Paragraph 0018-0041, (2019/10/01)

The invention discloses a method for syn...

Preparation method of chloromethyl hexafluoroisopropyl ether

-

Paragraph 0023; 0024; 0027; 0028, (2018/11/03)

The invention relates to a preparation m...

Method for synthesizing chloromethy-1,1,1,3,3,3-hexafluoroisopropyl ether

-

Paragraph 0018; 0019; 0020; 0021; 0022; 0023, (2016/12/22)

The invention discloses a method for syn...

Method for recycling sevoflurane impurity F(1)

-

Paragraph 0023; 0024; 0025; 0026; 0027; 0028-0038, (2017/07/22)

The invention discloses a method for rec...

26103-07-1 Process route

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

1,1,1,3',3',3'-hexafluoro-propanol
920-66-1

1,1,1,3',3',3'-hexafluoro-propanol

1,1,1,3,3,3-hexafluoroisopropyl chloromethyl ether
26103-07-1

1,1,1,3,3,3-hexafluoroisopropyl chloromethyl ether

Conditions
Conditions Yield
1,1,1,3',3',3'-hexafluoro-propanol; With aluminum (III) chloride; In acetonitrile; at 0 - 10 ℃; for 0.333333h; Inert atmosphere;
formaldehyd; In acetonitrile; at 15 ℃; for 6h; Temperature; Inert atmosphere;
93.2%
With aluminum (III) chloride; carbon dioxide; at 32 - 36 ℃; for 6h; under 60006 - 63756.4 Torr; Temperature; Autoclave;
92.7%
1,1,1,3',3',3'-hexafluoro-propanol; With aluminum (III) chloride; at -5 - 0 ℃; for 0.5h; Large scale;
formaldehyd; at 35 ℃; for 17h; Large scale;
With hydrogenchloride; In water; at 0 - 15 ℃; Large scale;
91.1%
With thionyl chloride; sulfuric acid; at 15 - 35 ℃; Product distribution / selectivity;
84.4%
With thionyl chloride; sulfuric acid; at 15 - 35 ℃; for 6h; Product distribution / selectivity;
26.0 - 84.4 %Chromat.
With thionyl chloride; sulfuric acid; at 20 ℃; for 6h; Product distribution / selectivity;
26.0 - 84.4 %Chromat.
C<sub>7</sub>H<sub>3</sub>F<sub>13</sub>O<sub>2</sub>

C7 H3 F13 O2

1,1,1,3,3,3-hexafluoroisopropyl chloromethyl ether
26103-07-1

1,1,1,3,3,3-hexafluoroisopropyl chloromethyl ether

Conditions
Conditions Yield
With 1,3,5-Trioxan; aluminum (III) chloride; at 10 ℃; for 12h; Temperature; Concentration;
90.6%
With hydrogenchloride; aluminum (III) chloride; formaldehyd; In water; at 5 ℃; for 6h; Temperature;

26103-07-1 Upstream products

  • 13171-18-1
    13171-18-1

    1,1,1,3,3,3-hexafluoro-2-methoxypropane

  • 110-88-3
    110-88-3

    1,3,5-Trioxan

  • 920-66-1
    920-66-1

    1,1,1,3',3',3'-hexafluoro-propanol

  • 28523-86-6
    28523-86-6

    sevoflurane

26103-07-1 Downstream products

  • 28523-86-6
    28523-86-6

    sevoflurane

  • 920-66-1
    920-66-1

    1,1,1,3',3',3'-hexafluoro-propanol

  • 206756-25-4
    206756-25-4

    2-Chloromethoxy-1,1,3,3,3-pentafluoro-propene

  • 1357476-59-5
    1357476-59-5

    bis-1,3-(1,1,1,3,3,3-hexafluoroiso-propoxymethyl)imidazolium chloride

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