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ETHYL 2-FLUOROBENZOATE

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Products Intro: Product Name:Ethyl 2-fluorobenzoate
CAS:443-26-5
Purity:98%(Min,HPLC) Package:1G;1KG;100KG
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Products Intro: Product Name: ETHYL 2-FLUOROBENZOATE
CAS: 443-26-5
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Products Intro: Product Name:ETHYL 2-FLUOROBENZOATE
CAS:443-26-5
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CAS:443-26-5
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Products Intro: Product Name:ETHYL 2-FLUOROBENZOATE
CAS:443-26-5
Purity:0.99 Package:5KG;1KG

ETHYL 2-FLUOROBENZOATE manufacturers

ETHYL 2-FLUOROBENZOATE Basic information
Product Name:ETHYL 2-FLUOROBENZOATE
Synonyms:RARECHEM AL BI 0016;2-fluoro-benzoicaciethylester;Ethyl 2-fluorobenzoate, 98+%;2-FLUOROBENZOIC ACID ETHYL ESTER;ETHYL 2-FLUOROBENZOATE;ETHYL O-FLUOROBENZOATE;Ethyl 2-fluorobenzoate 98%;2-FLUOROBENZOIC ACID ETHYL ESTER 96+%
CAS:443-26-5
MF:C9H9FO2
MW:168.16
EINECS:207-134-0
Product Categories:Benzoic acid;Acids & Esters;Fluorine Compounds;Aromatic Esters
Mol File:443-26-5.mol
ETHYL 2-FLUOROBENZOATE Structure
ETHYL 2-FLUOROBENZOATE Chemical Properties
Boiling point 115 °C
density 1.15
refractive index 1.493
Fp 217-220°C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light orange to Yellow
Specific Gravity1.15
BRN 2084296
CAS DataBase Reference443-26-5(CAS DataBase Reference)
EPA Substance Registry SystemBenzoic acid, 2-fluoro-, ethyl ester (443-26-5)
Safety Information
Hazard Codes F
Safety Statements 24/25
Hazard Note Flammable
TSCA TSCA listed
HS Code 29163990
MSDS Information
ProviderLanguage
ALFA English
ETHYL 2-FLUOROBENZOATE Usage And Synthesis
Chemical PropertiesClear colorless to yellow liquid
Synthesis
1-Fluoro-2-iodobenzene

348-52-7

potassium ethyl oxalate

1906-57-6

ETHYL 2-FLUOROBENZOATE

443-26-5

General procedure for the synthesis of ethyl o-fluorobenzoate from o-fluoroiodobenzene and potassium 2-ethoxy-2-oxoacetate: Palladium catalyst (1 mol%) and potassium 2-ethoxy-2-oxoacetate (0.75 mmol) were added to an oven-dried Schlenk tube (10 mL). The Schlenk tube was evacuated and backfilled with argon (this process was repeated three times). Subsequently, o-fluoroiodobenzene (0.5 mmol) and N-methylpyrrolidone (NMP, 1.0 mL) were added via syringe at room temperature under argon protection. After sealing the reaction vessel, it was placed in a preheated oil bath and reacted under stirring for 24 hours. Upon completion of the reaction, the mixture was cooled to room temperature, diluted with ethyl acetate and analyzed by gas chromatography.

References[1] Tetrahedron Letters, 2012, vol. 53, # 43, p. 5796 - 5799
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