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3',5'-Dichloroacetophenone

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Products Intro: Product Name:3',5'-Dichloroacetophenone
CAS:14401-72-0
Purity:98%(Min,GC) Package:1G;1KG;100KG
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Products Intro: Product Name:3',5'-Dichloroacetophenone
CAS:14401-72-0
Purity:99% Package:1KG,5KG,10KG
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Products Intro: Product Name:3',5'-Dichloroacetophenone
CAS:14401-72-0
Purity:99% Package:1KG;1USD
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Products Intro: Product Name:3',5'-Dichloroacetophenone
CAS:14401-72-0
Purity:98% Package:1kg,5kg,10kg Remarks:pharmaceutical intermediates

3',5'-Dichloroacetophenone manufacturers

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
EINECS:
Product Categories:Aromatic Acetophenones & Derivatives (substituted);Adehydes, Acetals & Ketones;Chlorine Compounds
Mol File:14401-72-0.mol
3',5'-Dichloroacetophenone Structure
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 Reference14401-72-0(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39-25/26
HS Code 29147000
MSDS Information
3',5'-Dichloroacetophenone Usage And Synthesis
Chemical PropertiesLight yellow liquid
Synthesis
3,5-Dichloroiodobenzene

3032-81-3

Acetic anhydride

108-24-7

3',5'-Dichloroacetophenone

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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