534595
4-(2-Methoxyethyl)phenol
97%
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About This Item
Linear Formula:
CH3O(CH2)2C6H4OH
CAS Number:
Molecular Weight:
152.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
260-354-9
MDL number:
Assay:
97%
InChI key
FAYGEALAEQKPDI-UHFFFAOYSA-N
InChI
1S/C9H12O2/c1-11-7-6-8-2-4-9(10)5-3-8/h2-5,10H,6-7H2,1H3
SMILES string
COCCc1ccc(O)cc1
assay
97%
mp
42-45 °C (lit.)
functional group
ether
Quality Level
Related Categories
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).
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
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
Regulatory Information
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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)
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)
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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