Skip to Content
Merck
All Photos(1)

Key Documents

534595

Sigma-Aldrich

4-(2-Methoxyethyl)phenol

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3O(CH2)2C6H4OH
CAS Number:
Molecular Weight:
152.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

mp

42-45 °C (lit.)

functional group

ether

SMILES string

COCCc1ccc(O)cc1

InChI

1S/C9H12O2/c1-11-7-6-8-2-4-9(10)5-3-8/h2-5,10H,6-7H2,1H3

InChI key

FAYGEALAEQKPDI-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

4-(2-Methoxyethyl)phenol can be prepared by reacting methyl vinyl ether and 4-bromonitrobenzene.

Application

4-(2-Methoxyethyl)phenol may be used in the preparation of methyl analog of metoprolol (MAM).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

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

Customers Also Viewed

Slide 1 of 2

1 of 2

A New Route to 4-(2-Methoxyethyl) Phenol Via Palladium-Catalysed Arylation of Methyl Vinyl Ether.
Hallberg A, et al.
Synthetic Communications, 15(13), 1131-1136 (1985)
Evidence that serine 304 is not a key ligand-binding residue in the active site of cytochrome P450 2D6.
Ellis SW, et al.
The Biochemical Journal, 345(3), 565-571 (2000)
Alfred Svan et al.
Journal of mass spectrometry : JMS, 51(3), 207-218 (2016-03-10)
Identification of degradation products from trace organic compounds, which may retain the biological activity of the parent compound, is an important step in understanding the long-term effects of these compounds on the environment. Constructed wetlands have been successfully utilized to
M Allaoua et al.
Journal of applied microbiology, 125(4), 1162-1174 (2018-05-18)
In vitro and in vivo studies were conducted to test a new carvacrol-based product designed to delay the carvacrol release so that it could reach the caeca of broiler chickens in order to control Campylobacter jejuni. Antimicrobial activity of carvacrol, a

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