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534595

Sigma-Aldrich

4-(2-Methoxyethyl)phenol

97%

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About This Item

Linear Formula:
CH3O(CH2)2C6H4OH
CAS Number:
56718-71-9
Molecular Weight:
152.19
EC Number:
260-354-9
MDL number:
MFCD00017537
UNSPSC Code:
12352100
PubChem Substance ID:
24878049
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

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

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General description

4-(2-Methoxyethyl)phenol can be prepared by reacting methyl vinyl ether and 4-bromonitrobenzene.[1]

Application

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ9217
MKCK8262
MKCB8704
MKBZ9545V
MKBZ9320V

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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)
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)
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
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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

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