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108057

Sigma-Aldrich

Methyl phenylacetate

ReagentPlus®, ≥99%

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About This Item

Fórmula lineal:
C6H5CH2CO2CH3
Número de CAS:
101-41-7
Peso molecular:
150.17
Beilstein/REAXYS Number:
878795
EC Number:
202-940-9
MDL number:
MFCD00008453
UNSPSC Code:
12352100
PubChem Substance ID:
24846797
NACRES:
NA.22

product line

ReagentPlus®

assay

≥99%

refractive index

n20/D 1.503 (lit.)

bp

218 °C (lit.)

density

1.066 g/mL at 20 °C (lit.)

SMILES string

COC(=O)Cc1ccccc1

InChI

1S/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3

InChI key

CRZQGDNQQAALAY-UHFFFAOYSA-N

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Application

Methyl phenylacetate was used as model compound for partition coefficient measurement experiments.

Biochem/physiol Actions

Methyl phenylacetate undergoes decomposition on photolysis in methanol. Methyl phenylacetate acts as acylating agent and causes the enantioselective acylation of beta-lactam intermediate using penicillin G amidase. Methyl phenylacetate is the starting material in manufacture of synthetic perfumes.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

211.1 °F - closed cup

flash_point_c

99.5 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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Photolysis of phenylacetic acid and methyl phenylacetate in methanol.
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Journal of the American Chemical Society, 94(6), 1989-1996 (1972)
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Enantioselective acylation of a beta-lactam intermediate in the synthesis of loracarbef using penicillin G amidase.
Zmijewski Jr MJ, et al.
Tetrahedron Letters, 32(13), 1621-1622 (1991)
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