Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

275638

Sigma-Aldrich

Methyl phenoxyacetate

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5OCH2CO2CH3
CAS Number:
2065-23-8
Molecular Weight:
166.17
EC Number:
218-176-4
MDL number:
MFCD00010227
UNSPSC Code:
12352100
PubChem Substance ID:
24856660
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.514 (lit.)

bp

243 °C (lit.)

density

1.149 g/mL at 25 °C (lit.)

SMILES string

COC(=O)COc1ccccc1

InChI

1S/C9H10O3/c1-11-9(10)7-12-8-5-3-2-4-6-8/h2-6H,7H2,1H3

InChI key

BZCKRPHEZOHHBK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Methyl phenoxyacetate (MPOA) was used as an acylating agent in the synthesis of loracarbef, a carbacephalosporin antibiotic[1].

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
96597KJ
15826CB
08517KZ
06121AV
05011KV

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service