Skip to Content
Merck
All Photos(2)

Key Documents

180653

Sigma-Aldrich

2-Methoxyphenylacetic acid

98%

Synonym(s):

(o-Methoxyphenyl)acetic acid, 2-Methoxybenzeneacetic acid, [2-(Methyloxy)phenyl]acetic acid, o-Anisylacetic acid, o-Methoxybenzeneacetic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3OC6H4CH2CO2H
CAS Number:
Molecular Weight:
166.17
Beilstein:
2047573
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

122-125 °C (lit.)

functional group

carboxylic acid

SMILES string

COc1ccccc1CC(O)=O

InChI

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

InChI key

IVEWTCACRDEAOB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

The cytotoxic potential of 2-methoxyphenylacetic acid was studied.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

242.6 °F - (External MSDS)

Flash Point(C)

117 °C - (External MSDS)

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

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.

Already Own This Product?

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

Visit the Document Library

Tiffany J Somers-Edgar et al.
Anti-cancer drugs, 20(1), 33-40 (2008-10-03)
We postulated that methoxy-substituted cyclic compounds could inhibit estrogen receptor (ER) negative breast cancer growth in vitro. Therefore, this study assessed the cytotoxic potential of various methoxy-substituted cyclic compounds [7,8-dimethoxyflavone, 4-methoxyphenylacetic acid, 2-methoxyphenylacetic acid, 4-methoxybenzophenone, 5-methoxy-1-indanone, and coenzyme Q0 (CoQ0)]

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