538-58-9

  • Product Name:Dibenzylideneacetone
  • Molecular Formula:C17H14O
  • Purity:99%
  • Molecular Weight:234.298
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Product Details

pd_meltingpoint:107-113 °C

Appearance:yellow powder

Purity:99%

Buy cost-effective 99% pure Dibenzylideneacetone 538-58-9 now

  • Molecular Formula:C17H14O
  • Molecular Weight:234.298
  • Appearance/Colour:yellow powder 
  • Vapor Pressure:1.25E-06mmHg at 25°C 
  • Melting Point:107-113 °C 
  • Refractive Index:1.649 
  • Boiling Point:400.7 °C at 760 mmHg 
  • Flash Point:176.2 °C 
  • PSA:17.07000 
  • Density:1.1 g/cm3 
  • LogP:3.98230 

DIBENZYLIDENEACETONE(Cas 538-58-9) Usage

Preparation

Dibenzylideneacetone is obtained by the reaction of benzaldehyde and acetone. The reaction was carried out in aqueous ethanol solution at a reaction temperature of 20-25°C with a yield of 78%.

Synthesis Reference(s)

Chemistry Letters, 9, p. 51, 1980The Journal of Organic Chemistry, 45, p. 3840, 1980 DOI: 10.1021/jo01307a022Organic Syntheses, Coll. Vol. 2, p. 167, 1943

Purification Methods

Crystallise the ketone from hot ethyl acetate (2.5mL/g) or EtOH. [Beilstein 7 IV 1747.]

InChI:InChI=1/C17H14O/c18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16/h1-14H/b13-11+,14-12u

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538-58-9 Process route

hydrogenchloride
7647-01-0,15364-23-5

hydrogenchloride

benzaldehyde
100-52-7

benzaldehyde

isopropyl alcohol
67-63-0,8013-70-5

isopropyl alcohol

benzyl chloride
100-44-7

benzyl chloride

1,5-diphenyl-1,4-pentadiene-3-one
538-58-9

1,5-diphenyl-1,4-pentadiene-3-one

Conditions
Conditions Yield
benzaldehyde
100-52-7

benzaldehyde

1,5-diphenyl-1,4-pentadiene-3-one
538-58-9

1,5-diphenyl-1,4-pentadiene-3-one

1-Phenylbut-1-en-3-one
122-57-6

1-Phenylbut-1-en-3-one

benzyl alcohol
100-51-6,185532-71-2

benzyl alcohol

Conditions
Conditions Yield
gadolinium(III) isopropoxide; In benzene; at 0 ℃; for 2h;
2.5%
0.6%
52%
With sodium 2,6-di-tert-butyl-4-methoxyphenolate; C23H21FeN5O2P(1+)*BF4(1-); isopropyl alcohol; In tetrahydrofuran; at 60 ℃; for 20h; Reagent/catalyst; Temperature; Catalytic behavior;
53 %Spectr.
22 %Spectr.
6 %Spectr.
With potassium tert-butylate; C23H21FeN5O2P(1+)*BF4(1-); isopropyl alcohol; In tetrahydrofuran; at 40 ℃; for 20h; Catalytic behavior;
17 %Spectr.
11 %Spectr.
9 %Spectr.
With C23H21FeN5O2P(1+)*BF4(1-); isopropyl alcohol; potassium hydroxide; In tetrahydrofuran; at 80 ℃; for 20h; Catalytic behavior;
35 %Spectr.
11 %Spectr.
7 %Spectr.

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