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3',5'-Dichloroacetophenone

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3',5'-Dichloroacetophenone Basic information

Product Name:
3',5'-Dichloroacetophenone
Synonyms:
  • Methyl 3,5-dichlorophenyl ketone
  • 1-(3,5-dichlorophenyl)ethan-1-one
  • 1-Acetyl-3,5-dichlorobenzene
  • 3',5'-Dichloroacetophenone≥ 98% (GC)
  • Ethanone, 1-(3,5-dichlorophenyl)-
  • Methanone,(6-methylphenyl)phenyl-
  • 3',5'-dichloroacetophenone
  • Ketoconazole Impurity 49
CAS:
14401-72-0
MF:
C8H6Cl2O
MW:
189.04
Product Categories:
  • Aromatic Acetophenones & Derivatives (substituted)
  • Adehydes, Acetals & Ketones
  • Chlorine Compounds
Mol File:
14401-72-0.mol
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3',5'-Dichloroacetophenone Chemical Properties

Melting point:
26 °C
Boiling point:
82°C 0,1mm
Density 
1.304±0.06 g/cm3(Predicted)
refractive index 
1.5630 to 1.5670
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow to Light orange
CAS DataBase Reference
14401-72-0(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-25/26
HS Code 
29147000
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3',5'-Dichloroacetophenone Usage And Synthesis

Chemical Properties

Light yellow liquid

Synthesis

3032-81-3

108-24-7

14401-72-0

General procedure for the synthesis of 1-(3,5-dichlorophenyl)ethanone from 3,5-dichloroiodobenzene (37.0 g, 136 mmol) and acetic anhydride: 3,5-dichloroiodobenzene, Pd2(dba)3 (1.5 g, 1.6 mmol), and lithium chloride (29.0 g, 682 mmol) were dissolved in 100 ml of DMF in a 500 ml round bottomed flask. Subsequently 64.0 ml of acetic anhydride and 47.0 ml of N-ethyl diisopropylamine were added to the reaction mixture. The reaction mixture was heated at 100°C for the reaction. After completion of the reaction, water was added to the mixture, extracted with ethyl acetate and the product was purified by column chromatography using ethyl acetate as eluent. 8 g of 1-(3,5-dichlorophenyl)ethanone was finally obtained.

References

[1] Patent: JP2015/212297, 2015, A. Location in patent: Paragraph 0106; 0107

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