1522-22-1

  • Product Name:Hexafluoroacetylacetone
  • Molecular Formula:C5H2F6O2
  • Purity:99%
  • Molecular Weight:208.06
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Product Details;

CasNo: 1522-22-1

Molecular Formula: C5H2F6O2

Appearance: clear colorless to slightly yellow liquid

factory and supplier 1522-22-1 Hexafluoroacetylacetone in stock

  • Molecular Formula:C5H2F6O2
  • Molecular Weight:208.06
  • Appearance/Colour:clear colorless to slightly yellow liquid 
  • Vapor Pressure:6.813mmHg at 25°C 
  • Refractive Index:n20/D 1.332(lit.)  
  • Boiling Point:70 °C at 760 mmHg 
  • PKA:4.30±0.10(Predicted) 
  • Flash Point:30.8 °C 
  • PSA:34.14000 
  • Density:1.506 g/cm3 
  • LogP:1.63930 

HEXAFLUOROACETYLACETONE(Cas 1522-22-1) Usage

Purification Methods

It forms a dihydrate which has no UV spectrum compared with max (CHCl3) 273nm ( 7,800) for the anhydrous ketone. The dihydrate decomposes at ~90o. The hydrate (10g) plus anhydous CaSO4 (Drierite, 30g) are heated and distilled, the distillate is treated with more CaSO4 and redistilled. When the distillate is treated with aqueous NaOH and heated, the dihydrate crystallises on cooling. The Cu complex has m 135o (after sublimation). [Gilman et al. J Am Chem Soc 78 2790 1956, Belford et al. J Inorg Nucl Chem 2 11 1956, Beilstein 1 IV 3681.]

General Description

**HEXAFLUOROACETYLACETONE (HFA)** is a fluorinated β-diketone commonly used as a ligand in coordination chemistry, particularly in the synthesis of metal complexes such as manganese(II) and cobalt(II) compounds. It serves as a chelating agent due to its ability to form stable complexes with transition metals, often contributing to the magnetic or cytotoxic properties of the resulting compounds. In the context of the provided literature, HFA is utilized in the preparation of antiferromagnetic manganese(II) complexes and cytotoxic cobalt(II) β-ketoaminato complexes, demonstrating its versatility in both materials science and medicinal chemistry applications.

InChI:InChI=1/C5H2F6O2/c6-1-2(12)4(7,8)3(13)5(9,10)11/h1H2

1522-22-1 Relevant articles

Method for Producing 1,1,1,5,5,5-Hexafluoroacetylacetone

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Paragraph 0124-0129, (2016/04/09)

A production method of a 1,1,1,5,5,5-hex...

PROCESSES FOR PRODUCING 1,1,1,5,5,5 HEXAFLUOROACETYL ACETONE

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Page/Page column 5-6, (2015/09/23)

The present invention relates to a proce...

METHOD FOR PRODUCING 1,1,1,5,5,5-HEXAFLUOROACETYLACETONE

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Paragraph 0150-0181, (2016/10/24)

A production method of a 1,1,1,5,5,5-hex...

Method for preparing chiral diphosphines

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, (2008/06/13)

The invention concerns a method for prep...

1522-22-1 Process route

1,1,1,5,5,5-hexafluoro-3-trifluoroacetyl-pentane-2,4-dione
72721-52-9

1,1,1,5,5,5-hexafluoro-3-trifluoroacetyl-pentane-2,4-dione

1,1,1,5,5,5-hexafluoroacetylacetone
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1,1,1,5,5,5-hexafluoroacetylacetone

trifluoroacetic acid
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trifluoroacetic acid

Conditions
Conditions Yield
With water; Title compound not separated from byproducts;
1,1,1,5,5,5-hexafluoro-3-trifluoromethyl-pentane-2,4-dione
69962-11-4

1,1,1,5,5,5-hexafluoro-3-trifluoromethyl-pentane-2,4-dione

trifluoromethyl 2,2,2-trifluororethyl ketone
400-49-7

trifluoromethyl 2,2,2-trifluororethyl ketone

1,1,1,5,5,5-hexafluoroacetylacetone
1522-22-1

1,1,1,5,5,5-hexafluoroacetylacetone

trifluoroacetic acid
76-05-1

trifluoroacetic acid

Conditions
Conditions Yield
With water; Title compound not separated from byproducts; 1.) 20 deg C, 7 d, 2.) 100 - 110 deg C, 70 h;

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