375-50-8

  • Product Name:1,4-Diiodooctafluorobutane
  • MF:C4F8 I2
  • Purity:99%
  • Molecular Weight:453.84
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Product Details

Cost-effective customized wholesale 1,4-Diiodooctafluorobutane 375-50-8

  • Molecular Formula:C4F8 I2
  • Molecular Weight:453.84
  • Appearance/Colour:liquid 
  • Vapor Pressure:6.02mmHg at 25°C 
  • Melting Point:−9 °C(lit.)
     
  • Refractive Index:n20/D 1.429(lit.) 
  • Boiling Point:150 °C(lit.)
     
  • Flash Point:55.9°C 
  • PSA:0.00000 
  • Density:2.474 
  • LogP:4.31260 

1,4-Diiodooctafluorobutane(Cas 375-50-8) Usage

General Description

Octafluoro-1,4-diiodobutane (ofib, C4F8I2) is also referred to as 1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane. It acts as a halogen bond donor compound and its cocrystallization with methyldiphenylphosphine oxide (mdppo) has been investigated. In combination with a calixcrown compound ofib forms a ′binary host′ system, which is employed for the isolation of cesium iodide from aqueous to fluorous phase.

InChI:InChI=1/C4F8I2/c5-1(6,3(9,10)13)2(7,8)4(11,12)14

375-50-8 Relevant articles

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Hauptschein et al.

, p. 1974 (1952)

-

Preparation and characterization of a halogen-bonded shape-persistent chiral alleno-acetylenic inclusion complex

Castro-Fernandez, Silvia,Lahoz, Inmaculada R.,Llamas-Saiz, Antonio L.,Alonso-Gomez, Jose Lorenzo,Cid, Maria-Magdalena,Navarro-Vazquez, Armando

, p. 1136 - 1139 (2014)

A chiral bidentate inclusion complex has...

Synthesis of fluorinated telomers. Part 4. Telomerization of vinylidene fluoride with commercially available α,ω-diiodoperfluoroalkanes

Manseri, Abdellatif,Ameduri, Bruno,Boutevin, Bernard,Chambers, Richard D.,Caporiccio, Gerardo,Wright, Anthony P.

, p. 59 - 68 (1995)

The synthesis of a new fluorinated α,ω-d...

Fluorine-containing compound, and its manufacturing method (by machine translation)

-

Paragraph 0039; 0040, (2017/01/02)

PROBLEM TO BE SOLVED: perfluoroalkyl gro...

PARTIALLY FLUORINATED COMPOUNDS

-

Paragraph 0105-0106, (2014/07/07)

Described herein is a composition compri...

PROCESS FOR THE PURIFICATION OF ALPHA, OMEGA-DIIODOPERFLUORINATED COMPOUNDS

-

Page/Page column 5, (2010/08/08)

The invention concerns a process for pur...

375-50-8 Process route

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

polytetrafluoroethylene

(Z)-perfluoro-2-butene
1516-65-0

(Z)-perfluoro-2-butene

Pentafluoroethyl iodide
354-64-3

Pentafluoroethyl iodide

1,2-diiodotetrafluoroethane
354-65-4

1,2-diiodotetrafluoroethane

1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
423-39-2

1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane

1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane
375-50-8

1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane

Conditions
Conditions Yield
With iodine; antimony(III) fluoride; iodine pentafluoride; at 40 ℃; for 7h; Rate constant; Product distribution; Kinetics; mechanism; var. temp., pressures, and C2F4 : I2 : IF5 molar ratios; other fluoroolefins with I2-IF5-SbF3, selectivity of formation, thermal effect;
1,1,2,2,3,3,4,4-Octafluoro-butane-1,4-disulfinic acid

1,1,2,2,3,3,4,4-Octafluoro-butane-1,4-disulfinic acid

1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane
375-50-8

1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane

Conditions
Conditions Yield
With sodium persulfate; iodine; In water; isopropyl alcohol; at 55 - 75 ℃; for 2h;
147 g

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