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2-Fluorophenylacetone

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  • 2025-06-20
  • CAS:2836-82-0
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  • Purity: 0.99
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2-Fluorophenylacetone Basic information
Product Name:2-Fluorophenylacetone
Synonyms:2-FLUOROPHENYLACETONE;2-FLUOROPHENYLACETONE 99% (GC);2-Fluorophenylacetone 99%;2-Fluorophenylacetone99%;o-Fluorophenylacetone;1-(2-Fluorophenyl)acetone;(o-Fluorophenyl)-2-propanone;1-(o-Fluorophenyl)-2-propanone
CAS:2836-82-0
MF:C9H9FO
MW:152.17
EINECS:220-627-5
Product Categories:C9;Carbonyl Compounds;Ketones;Aromatic Ketones (substituted);2836-82-0
Mol File:2836-82-0.mol
2-Fluorophenylacetone Structure
2-Fluorophenylacetone Chemical Properties
Boiling point 47 °C/0.05 mmHg (lit.)
density 1.077 g/mL at 25 °C (lit.)
refractive index n20/D 1.4989(lit.)
Fp 185 °F
storage temp. Sealed in dry,Room Temperature
solubility Methyl Acetate: 50 mg/ml
form Liquid
color Pale yellow
InChIInChI=1S/C9H9FO/c1-7(11)6-8-4-2-3-5-9(8)10/h2-5H,6H2,1H3
InChIKeyBANVZEUCJHUPOI-UHFFFAOYSA-N
SMILESC(C1=CC=CC=C1F)C(=O)C
CAS DataBase Reference2836-82-0(CAS DataBase Reference)
Safety Information
Hazard Codes F
Risk Statements 36/37/38
Safety Statements 24/25
WGK Germany 3
Hazard Note Flammable
HS Code 2914.39.9000
MSDS Information
ProviderLanguage
1-(2-Fluorophenyl)acetone English
SigmaAldrich English
ACROS English
2-Fluorophenylacetone Usage And Synthesis
Chemical Propertiesclear light yellow liquid
Uses2-Fluorophenylacetone is used in the synthesis of antimalarial drugs.
Uses(2-Fluorophenyl)acetone was used in the synthesis of 6-methyluracils.
General Description(2-Fluorophenyl)acetone on reaction with chlorosulfonyl isocyanate yields 5-(2-fluorophenyl)-6-methyl-1,3-oxazine-2,4-(3H)-dione.
Synthesis
1-(2-FLUOROPHENYL)-2-NITROPROPENE

829-40-3

2-Fluorophenylacetone

2836-82-0

General procedure for the synthesis of 2-o-fluoropropiophenone from (2-fluorophenyl)-2-nitropropene: a suspension of 1-fluoro-2-(2-nitroprop-1-en-1-yl)benzene (2054547) (160 g, 0.88 mol), powdered iron (320 g, 5.71 mol) and ferric(III) chloride (3.2 g, 19.6 mmol) in 640 ml of water, was heated to 80°C with stirring and 37% hydrochloric acid (320 ml) was added slowly over a period of 20 min. Subsequently, the reaction mixture was heated to reflux state kept for 1 hour and then cooled to room temperature. Ethyl acetate (1 L) was added and the mixture was filtered through a diatomaceous earth pad to separate the organic and aqueous layers. The organic layer was dried and concentrated and the crude product obtained was purified by distillation under reduced pressure to give 1-(2-fluorophenyl)propan-2-one (2054549) (90 g, 67% yield) with Rf = 0.40 (ethyl acetate:heptane = 1:4) and a boiling point of 70 °C (1 mmHg).

References[1] Patent: WO2017/29104, 2017, A1. Location in patent: Page/Page column 12
[2] Chimica Therapeutica, 1968, vol. 3, p. 313 - 320
Tag:2-Fluorophenylacetone(2836-82-0) Related Product Information
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