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Merck
CN

05010

Ethyl vinyl ether

purum, ≥98.0% (GC)

Synonym(s):

Ethoxyethylene

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About This Item

Linear Formula:
C2H5OCH=CH2
CAS Number:
Molecular Weight:
72.11
NACRES:
NA.23
PubChem Substance ID:
eCl@ss:
39021025
UNSPSC Code:
12162002
MDL number:
Beilstein/REAXYS Number:
605351
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Product Name

Ethyl vinyl ether, purum, ≥98.0% (GC)

InChI

1S/C4H8O/c1-3-5-4-2/h3H,1,4H2,2H3

SMILES string

CCOC=C

InChI key

FJKIXWOMBXYWOQ-UHFFFAOYSA-N

grade

purum

assay

≥98.0% (GC)

form

liquid

contains

~0.1% diethylaniline as stabilizer

refractive index

n20/D 1.376 (lit.)
n20/D 1.376

bp

33 °C (lit.)

mp

−116 °C (lit.)

density

0.753 g/mL at 25 °C (lit.)

Quality Level

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pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Flam. Liq. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

-49.0 °F

flash_point_c

-45 °C

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

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Laurance G Beauvais et al.
Journal of the American Chemical Society, 127(20), 7370-7378 (2005-05-19)
Soluble methane monooxygenase (sMMO) isolated from Methylococcus capsulatus (Bath) utilizes a carboxylate-bridged diiron center and dioxygen to catalyze the conversion of methane to methanol. Previous studies revealed that a di(mu-oxo)diiron(IV) intermediate termed Q is responsible for the catalytic activity with
Guotao Li et al.
Journal of the American Chemical Society, 130(22), 6944-6945 (2008-05-10)
An efficient Au(I)-catalyzed synthesis of highly strained and functionalized bicyclo[3.2.0]heptanes is developed. Subsequent couplings with various nucleophiles offer additional structural features/complexity. These one-pot, three-component reactions are proposed to proceed via a key 1,3-dipolar cycloaddition between a Au carbenoid-containing carbonyl ylide
Natalia Chernyak et al.
Journal of the American Chemical Society, 134(30), 12466-12469 (2012-07-21)
Anilines and ethyl vinyl ether can be used as precursors for a process that is the synthetic equivalent of the α-arylation of acetaldehyde enolate. The reaction manifests a high level of functional group compatibility, allowing the ready preparation of a
Eden Tesfu et al.
Journal of the American Chemical Society, 128(1), 70-71 (2006-01-05)
A Pd(II) reagent has been generated at preselected sites on an electrochemically addressable chip and used to effect the oxidation of the neighboring alcohols on the polymer coating the chip's surface. The resulting carbonyls were then used to accomplish site-selective
Shouming Zhou et al.
The journal of physical chemistry. A, 110(23), 7386-7392 (2006-06-09)
Kinetic studies on the gas-phase reactions of OH and NO3 radicals and ozone with ethyl vinyl ether (EVE), propyl vinyl ether (PVE) and butyl vinyl ether (BVE) have been performed in a 405 L borosilicate glass chamber at 298 +/-

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