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2-Fluoro-4-methoxyacetophenone

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Products Intro: Product Name:2-Fluoro-4-methoxyacetophenone
CAS:74457-86-6
Purity:98%(Min,GC) Package:1G;1KG;100KG
Company Name: Shanghai Daken Advanced Materials Co.,Ltd
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Products Intro: Product Name:2'-Fluoro-4'-methoxyacetophenone
CAS:74457-86-6
Purity:99% Package:1KG,5KG,10KG
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Products Intro: Product Name:2'-Fluoro-4'-methoxyacetophenone
CAS:74457-86-6
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Products Intro: Product Name:2'-Fluoro-4'-methoxyacetophenone
CAS:74457-86-6
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Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:2'-fluoro-4'-methoxyacetophenone
CAS:74457-86-6
Purity:99% Package:1kg

2-Fluoro-4-methoxyacetophenone manufacturers

2-Fluoro-4-methoxyacetophenone Basic information
Product Name:2-Fluoro-4-methoxyacetophenone
Synonyms:2'-Fluoro-4'-Methoxyacetoph...;Ethanone, 1-(2-fluoro-4-Methoxyphenyl)-;2'-Fluoro-4'-methoxylacetophenone;2-FLUORO-4-METHOXYACETOPHENONE;1-(2-FLUORO-4-METHOXYPHENYL)ETHANONE;4-ACETYL-3-FLUOROANISOLE;2-FLUORO-4-METHOXYACETOPHENONE 99% (HP&;2-FLUORO-4-METHXOYACETOPHENONE
CAS:74457-86-6
MF:C9H9FO2
MW:168.16
EINECS:
Product Categories:Aromatic Acetophenones & Derivatives (substituted);Adehydes, Acetals & Ketones;Anisoles, Alkyloxy Compounds & Phenylacetates;Fluorine Compounds;C9;Carbonyl Compounds;Ketones;Fluorine series
Mol File:74457-86-6.mol
2-Fluoro-4-methoxyacetophenone Structure
2-Fluoro-4-methoxyacetophenone Chemical Properties
Melting point 52-54 °C(lit.)
Boiling point 80-85 °C (0.1 mmHg)
density 1.1410 (estimate)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
form Viscous Solution
color Clear colorless
Water Solubility Insoluble
BRN 3539992
CAS DataBase Reference74457-86-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 29147000
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2-Fluoro-4-methoxyacetophenone Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses2′-Fluoro-4′-methoxyacetophenone may be used in chemical synthesis.
PreparationObtained by reaction of acetic anhydride with 3-fluoroanisole in the presence of aluminium chloride in carbon disulfide at r.t., then at 30–35° until no more hydrochloric acid is evolved.
Synthesis
Ethanone, 1-(2-fluoro-4-methoxyphenyl)-, O-methyloxime

1313430-15-7

2-Fluoro-4-methoxyacetophenone

74457-86-6

3-Fluoro-4-methoxyacetophenone oxime ether (39.4 mg, 0.2 mmol) was dissolved in 2 mL of ether, 37% hydrochloric acid was added and the reaction was stirred for 30 h at room temperature. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction solution was neutralized with saturated sodium carbonate solution to pH 7, followed by extraction of the mixture with ether (10 mL × 3). The organic phases were combined, dried with anhydrous sodium sulfate, and concentrated under reduced pressure to remove the solvent. The crude product was purified by column chromatography (eluent ratio: petroleum ether/ethyl acetate = 20:1, v/v), and the eluent containing the target product was collected, and the solvent was removed by distillation under reduced pressure to afford 2-fluoro-4-methoxyacetophenone (26.5 mg, 79% yield).

References[1] Patent: CN103922904, 2016, B. Location in patent: Paragraph 0058; 0059; 0062
Tag:2-Fluoro-4-methoxyacetophenone(74457-86-6) Related Product Information
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