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Merck

240095

Ethyl vinyl ether

≥99%

Sinónimos:

Ethoxyethylene

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About This Item

Fórmula lineal:
C2H5OCH=CH2
Número de CAS:
Peso molecular:
72.11
Beilstein/REAXYS Number:
605351
MDL number:
UNSPSC Code:
12352112
PubChem Substance ID:

assay

≥99%

contains

0.1% triethanolamine as stabilizer

refractive index

n20/D 1.376 (lit.)

bp

33 °C (lit.)

mp

−116 °C (lit.)

density

0.753 g/mL at 25 °C (lit.)

storage temp.

2-8°C

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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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
O Schalk et al.
The journal of physical chemistry. A, 119(45), 11105-11112 (2015-10-23)
A series of different alkyl vinyl ethers is investigated to decipher the possible reaction channels upon photoexcitation to the π3s-Rydberg and the ππ*-valence state at 200 nm using time-resolved photoelectron spectroscopy and on-the-fly time-dependent density functional theory dynamics simulations. The
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
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
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

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