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241989

Sigma-Aldrich

Ethoxybenzene

99%

Synonym(s):

Phenetole, Ethoxybenzene, Ethyl phenyl ether

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About This Item

Linear Formula:
C6H5OC2H5
CAS Number:
103-73-1
Molecular Weight:
122.16
Beilstein:
636270
EC Number:
203-139-7
MDL number:
MFCD00009090
UNSPSC Code:
12352100
PubChem Substance ID:
24854525
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.507 (lit.)

bp

169-170 °C (lit.)

mp

−30 °C (lit.)

solubility

alcohol: freely soluble(lit.)
diethyl ether: freely soluble(lit.)
water: insoluble(lit.)

density

0.966 g/mL at 25 °C (lit.)

functional group

phenoxy

SMILES string

CCOc1ccccc1

InChI

1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3

InChI key

DLRJIFUOBPOJNS-UHFFFAOYSA-N

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Application

Ethoxybenzene (Phenetole) was used as an analyte in assaying the performance of the porous graphitic carbon (PGC) particles.

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

134.6 °F - closed cup

Flash Point(C)

57 °C - closed cup

Certificates of Analysis (COA)

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Niklas Helle et al.
European journal of mass spectrometry (Chichester, England), 25(1), 142-156 (2019-02-19)
The vibronic structure of the first electronically excited state S1 and ionic ground state D0 of phenetole has been investigated by means of resonance enhanced multi photon ionization (REMPI) and mass analyzed threshold ionization (MATI) spectroscopy. The vibronic levels were
Wojciech Piatkowski et al.
Journal of chromatography. A, 1003(1-2), 73-89 (2003-08-06)
The competitive adsorption behavior of the binary mixture of phenetole (ethoxy-benzene) and propyl benzoate in a reversed-phase system was investigated. The adsorption equilibrium data of the single-component systems were acquired by frontal analysis. The same data for binary mixtures were
David S Jensen et al.
Journal of chromatography. A, 1218(46), 8362-8369 (2011-10-19)
Porous graphitic carbon (PGC) particles were functionalized/passivated in situ in packed beds at elevated temperature with neat di-tert-amylperoxide (DTAP) in a column oven. The performance of these particles for high performance liquid chromatography (HPLC) was assayed before and after this
Isamu Shiina et al.
Bioorganic & medicinal chemistry, 15(24), 7599-7617 (2007-10-02)
Two new synthetic pathways to the anti-cancer agent tamoxifen and its derivatives were developed. The first route involved the aldol reaction of benzyl phenyl ketone with acetaldehyde followed by Friedel-Crafts substitution with anisole in the presence of Cl(2)Si(OTf)(2) to produce
H Ohi et al.
Xenobiotica; the fate of foreign compounds in biological systems, 22(11), 1329-1337 (1992-11-01)
1. The effects of oxygen concentration were studied on the metabolic pathways of anisole homologues (anisole, phenetole and isopropoxybenzene) catalysed by liver microsomes from phenobarbital-treated rats. 2. With increase of oxygen concentration, the rate of anisole o-hydroxylation reached a plateau
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