Methyl phenoxyacetate

Methyl phenoxyacetate Basic information
Product Name:Methyl phenoxyacetate
Synonyms:METHYL PHENOXYACETATE;PHENOXYACETIC ACID METHYL ESTER;PHENOXY METHYL ACETATE;Acetic acid, phenoxy-, methyl ester;Methyl(ethyl)phenoxyacetate;Phenoxyacetic acid methyl;Methyl phenoxyacetate,99%;phenoxy-aceticacimethylester
CAS:2065-23-8
MF:C9H10O3
MW:166.17
EINECS:218-176-4
Product Categories:Building Blocks;C8 to C9;C8 to C9;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Carbonyl Compounds;Esters
Mol File:2065-23-8.mol
Methyl phenoxyacetate Structure
Methyl phenoxyacetate Chemical Properties
Melting point 245 °C
Boiling point 243 °C (lit.)
density 1.149 g/mL at 25 °C (lit.)
refractive index n20/D 1.514(lit.)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light orange to Yellow
Specific Gravity1.149
InChIKeyBZCKRPHEZOHHBK-UHFFFAOYSA-N
LogP1.410
CAS DataBase Reference2065-23-8(CAS DataBase Reference)
NIST Chemistry ReferenceAcetic acid, phenoxy-, methyl ester(2065-23-8)
EPA Substance Registry SystemAcetic acid, phenoxy-, methyl ester (2065-23-8)
Safety Information
Safety Statements 24/25
WGK Germany 3
TSCA T
HS Code 29189900
MSDS Information
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Methyl phenoxyacetate English
SigmaAldrich English
ACROS English
Methyl phenoxyacetate Usage And Synthesis
Chemical PropertiesMethyl phenoxyacetate, when the temperature ≥ 30°C is a clear colorless to slightly yellow liquid; at < 30°C is a white solid. It can be used as disinfectant or pharmaceutical intermediate or pesticide intermediate.
UsesMethyl phenoxyacetate (MPOA) was used as an acylating agent in the synthesis of loracarbef, a carbacephalosporin antibiotic.
Preparationsynthesis of methyl phenoxyacetate: methyl bromoacetate (10 mL, 105.6 mmol) and phenol (9.9380 g, 105.6 mmol) were dissolved in 250 mL of acetone; K2CO3 (21.89 g, 158 mmol) and KI (5 g, 30 mmol) were added and the mixture heated to reflux with stirring overnight. The mixture was filtered and the resultant solution concentrated in vacuo. Deionized water (200 mL) was added. The reaction mixture was extracted with 50 mL ethyl acetate three times. The combined ethyl acetate layers were washed with brine, dried over MgSO4, and filtered. All ethyl acetate was removed in vacuo, resulting in a slightly yellow liquid (80% yield).
Methyl phenoxyacetate Methylparaben Methyl Methyl phenylacetate Methyl glycolate Bensulfuron methyl Parathion-methyl Phenoxyacetic acid Kresoxim-methyl Methyl bromoacetate Methyl methoxyacetate Thiophanate-methyl METHYL Α-NAPHTHYLACETATE Methyl acrylate Methyl acetate Methyl bromide METSULFURON METHYL Methyl cyanoacetate

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