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05010

Sigma-Aldrich

Ethyl vinyl ether

purum, ≥98.0% (GC)

Synonym(s):

Ethoxyethylene

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About This Item

Linear Formula:
C2H5OCH=CH2
CAS Number:
109-92-2
Molecular Weight:
72.11
Beilstein:
605351
MDL number:
MFCD00009248
UNSPSC Code:
12162002
eCl@ss:
39021025
PubChem Substance ID:
329748004
NACRES:
NA.23

grade

purum

Quality Level

100

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.)

SMILES string

CCOC=C

InChI

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

InChI key

FJKIXWOMBXYWOQ-UHFFFAOYSA-N

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Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H336,H412

Hazard Classifications

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

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

-49.0 °F

Flash Point(C)

-45 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD6035
BCBT9649

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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
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
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
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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