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647-42-7

  • Product Name1H,1H,2H,2H-PERFLUORO-1-OCTANOL
  • Molecular FormulaC8H5F13O
  • Molecular Weight364.106
  • Purity99%
  • AppearanceColorless liquid
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Product Details

Quick Details

  • CasNo: 647-42-7
  • Molecular Formula: C8H5F13O
  • Appearance: Colorless liquid
  • Purity: 99%

Chinese Manufacturer Supply 99% Pure 1H,1H,2H,2H-PERFLUORO-1-OCTANOL 647-42-7 In Bulk Supply

  • Molecular Formula:C8H5F13O
  • Molecular Weight:364.106
  • Appearance/Colour:Colorless liquid 
  • Vapor Pressure:0.382mmHg at 25°C 
  • Refractive Index:n20/D 1.313(lit.)  
  • Boiling Point:174.1 °C at 760 mmHg 
  • PKA:14.26±0.10(Predicted) 
  • Flash Point:91.667 °C 
  • PSA:20.23000 
  • Density:1.589 g/cm3 
  • LogP:4.10760 

3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluoro-1-octanol(Cas 647-42-7) Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

Uses

1H,1H,2H,2H-Perfluoro-1-octanol is a material used to improve nanotube composites. It is also used in the synthesis of a recyclable fluorous hydrazine carbothioate compound with NCS to catalyz e the acetalization of aldehydes.

General Description

1H,1H,2H,2H-Perfluoro-1-octanol is a fluorotelomer alcohol.

InChI:InChI=1/C8H5F13O/c9-3(10,1-2-22)4(11,12)5(13,14)6(15,16)7(17,18)8(19,20)21/h22H,1-2H2

647-42-7 Relevant articles

Further evidence on the importance of fluorous-fluorous interactions in supramolecular chemistry: A combined structural and computational study

Omorodion, Harrison,Twamley, Brendan,Platts, James A.,Baker, Robert J.

, p. 2835 - 2841 (2015)

The solid-state structures of CF3(CF2)5C...

Environmentally friendly preparation method of fluorine-containing acrylate

-

Paragraph 0024; 0027, (2019/01/06)

The invention relates to the technical f...

Method for preparing perfluoroalkyl ethanol

-

Paragraph 0026-0032, (2017/11/29)

The invention discloses a method for pre...

Perfluoroalkyl ethyl alcohols via perfluoroalkyl acetaldehydes

Peng, Sheng,Moloy, Kenneth G.

, p. 7 - 10 (2017/08/04)

A new route to commercially important pe...

Method for preparing perfluoroalkyl alcohol from perfluoroalkyl ethylene

-

Paragraph 0026; 0028; 0029, (2017/04/03)

The invention discloses a method for pre...

647-42-7 Process route

1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane
2043-57-4,71215-70-8

1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane

1H,1H,2H,2H-tridecafluoro-n-octanol
647-42-7

1H,1H,2H,2H-tridecafluoro-n-octanol

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene
25291-17-2

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene

(perfluoro-n-hexyl)ethane
80793-17-5

(perfluoro-n-hexyl)ethane

Conditions
Conditions Yield
With water; lithium chloride; In N,N-dimethyl-formamide; Product distribution; effect of quantity of water and current on electroreduction;
80 % Spectr.
5 % Spectr.
15 % Spectr.
3,4-Dihydro-5-<(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro)octyloxy>-2H-pyrrole
155939-24-5

3,4-Dihydro-5-<(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro)octyloxy>-2H-pyrrole

2-pyrrolidinon
616-45-5

2-pyrrolidinon

1H,1H,2H,2H-tridecafluoro-n-octanol
647-42-7

1H,1H,2H,2H-tridecafluoro-n-octanol

1-(1-pyrrolin-2-yl)-2-pyrrolidinone
7060-52-8

1-(1-pyrrolin-2-yl)-2-pyrrolidinone

Conditions
Conditions Yield
With hydrogenchloride; In chloroform-d1; acetone; at 25 - 30 ℃; for 3h; Product distribution; other duration;
6.40 % Chromat.
0.147 % Chromat.
2.66 % Chromat.

647-42-7 Upstream products

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    123-39-7

    N-Methylformamide

  • 2043-57-4
    2043-57-4

    1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane

  • 16741-46-1
    16741-46-1

    N-isopropylformamide

  • 4938-92-5
    4938-92-5

    N-(2-formylaminoethyl)formamide

647-42-7 Downstream products

  • 2144-53-8
    2144-53-8

    3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-methylpropenoate

  • 141564-12-7
    141564-12-7

    3',3',4',4',5',5',6',6',7',7',8',8',8'-tridecafluorooctyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside

  • 141564-11-6
    141564-11-6

    3',3',4',4',5',5',6',6',7',7',8',8',8'-tridecafluorooctyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside

  • 64018-25-3
    64018-25-3

    3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanoyl chloride