4-(2-Methoxyethyl)phenol

Name: 4-(2-Methoxyethyl)phenol
Brand: ALDRICH
Price: 69.8 USD

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

Key Documents

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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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Show Differences

1 of 4

This Item	525553	422916	12268
Sigma-Aldrich 534595 4-(2-Methoxyethyl)phenol	Sigma-Aldrich 525553 4-Phenyl-1-(2H)-phthalazinone	Sigma-Aldrich 422916 2-Methoxy-4-nitrobenzoic acid	Sigma-Aldrich 12268 Ethyl benzimidate hydrochloride
assay 97%	assay 97%	assay 98%	assay ≥97.0% (AT)
Quality Level 100	Quality Level 100	Quality Level 200	Quality Level 100
mp 42-45 °C (lit.)	mp 240-244 °C (lit.)	mp 146-148 °C (lit.)	mp ~125 °C (dec.)
functional group ether	functional group phenyl	functional group carboxylic acid, nitro	functional group ether, phenyl

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

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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)

Pharmacokinetic and antimicrobial activity of a new carvacrol-based product against a human pathogen, Campylobacter jejuni.

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

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)

Identification of transformation products from β-blocking agents formed in wetland microcosms using LC-Q-ToF.

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

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