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Catalysts&Auxiliary Agents

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Bisphenol AF

  • Product Name: Bisphenol AF
  • CAS: 1478-61-1
  • Purity:
  • Appearance: White to off-white powder

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Factory supply good quality Bisphenol AF 1478-61-1 with stock

  • Molecular Formula:C15H10F6O2
  • Molecular Weight:336.234
  • Appearance/Colour:White to off-white powder 
  • Vapor Pressure:0.001mmHg at 25°C 
  • Melting Point:160-163 °C(lit.) 
  • Refractive Index:1.473 
  • Boiling Point:344.1 °C at 760 mmHg 
  • PKA:8.74±0.10(Predicted) 
  • Flash Point:161.9 °C 
  • PSA：40.46000 
  • Density:1.447 g/cm3 
  • LogP:4.50850 

Hexafluorobisphenol A(Cas 1478-61-1) Usage

Hazard

Moderately toxic by ingestion.

Flammability and Explosibility

Notclassified

Definition

ChEBI: An organofluorine compound that is bisphenol A with its methyl hydrogens replaced by fluorines.

InChI:InChI=1/C15H10F6O2/c1-15(2,7-3-5-8(22-20)6-4-7)9-10(16)12(18)14(23-21)13(19)11(9)17/h3-6H,1-2H3

1478-61-1 Relevant articles

Organized surface functional groups: Cooperative catalysis via thiol/sulfonic acid pairing

Margelefsky, Eric L.,Zeidan, Ryan K.,Dufaud, Veronique,Davis, Mark E.

, p. 13691 - 13697 (2007)

The synthesis and characterization of he...

HF-mediated equilibrium between fluorinated ketones and the corresponding α-fluoroalcohols

Hayasaka, Tatsuya,Katsuhara, Yutaka,Kume, Takashi,Yamazaki, Takashi

, p. 2215 - 2219 (2011)

We have successfully obtained the first ...

Synthetic method of hexafluorobisphenol A

-

Paragraph 0030; 0032; 0033; 0034; 0036; 0037; 0039, (2020/04/17)

The invention provides a synthetic metho...

A diaryl hexafluoropropane synthetic method of the compound

-

Paragraph 0013; 0019; 0027-0034, (2017/04/11)

The invention provides a method for synt...

Diaryl hexafluoroacetore the synthetic method of the compound of

-

Paragraph 0039-0040, (2017/02/09)

The invention provides of a synthesis me...

2, 2-bis (4-hydroxyphenyl) propane hexafluoroisopropylether manufacturing method (by machine translation)

-

Paragraph 0021; 0042-0056, (2018/11/22)

The invention provides a method for manu...

1478-61-1 Process route

Hexafluoroacetone
684-16-2

Hexafluoroacetone

phenol
108-95-2,27073-41-2

phenol

4,4'-(hexafluoroisopropylidene)diphenol
1478-61-1

4,4'-(hexafluoroisopropylidene)diphenol

Conditions
Conditions Yield
With hydrogen fluoride; In melt; at 10 - 100 ℃; for 2h; Temperature; Autoclave;
95%
With hydrogen fluoride;
 
surface-bound sulfonic acid-containing material; at 90 ℃; for 24h;
 
heptafluoropropan-2-ol
24427-67-6

heptafluoropropan-2-ol

phenol
108-95-2,27073-41-2

phenol

4,4'-(hexafluoroisopropylidene)diphenol
1478-61-1

4,4'-(hexafluoroisopropylidene)diphenol

Conditions
Conditions Yield
With hydrogen fluoride; at 110 ℃; for 6h; under 7125.71 Torr; Autoclave;
82%

1478-61-1 Upstream products

  • 684-16-2
    684-16-2

    Hexafluoroacetone

  • 108-95-2
    108-95-2

    phenol

  • 24427-67-6
    24427-67-6

    heptafluoropropan-2-ol

  • 428-59-1
    428-59-1

    Hexafluoropropene oxide

1478-61-1 Downstream products

  • 117583-45-6
    117583-45-6

    Propynoic acid 4-[2,2,2-trifluoro-1-(4-propynoyloxy-phenyl)-1-trifluoromethyl-ethyl]-phenyl ester

  • 83558-77-4
    83558-77-4

    2,2-bis(4-trifluoromethanesulfonyloxyphenyl)hexafluoropropane

  • 137999-86-1
    137999-86-1

    2,2-bis<(p-3'-fluoro-4'-nitrophenyl-carbamato)phenyl>-1,1,1,3,3,3-hexafluoropropane

  • 82986-78-5
    82986-78-5

    2,2-bis(4-allyloxyphenyl)hexafluoropropane

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