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05010

Ethyl vinyl ether

Name: Ethyl vinyl ether
Brand: SIAL

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

NACRES:

NA.23

PubChem Substance ID:

329748004

eCl@ss:

39021025

UNSPSC Code:

12162002

MDL number:

MFCD00009248

Beilstein/REAXYS Number:

605351

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Properties

grade

purum

Quality Level

100

assay

≥98.0% (GC)

form

liquid

contains

~0.1% diethylaniline as stabilizer

refractive index

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

Description

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pictograms

GHS02,GHS07

signalword

Danger

hcodes

H225,H336,H412

pcodes

P210 - P233 - P240 - P241 - P242 - P273

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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Certificates of Analysis (COA)

Lot/Batch Number

BCCD6035

BCBT9649

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Continuous-flow synthesis of monoarylated acetaldehydes using aryldiazonium salts.

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

Au(I)-catalyzed efficient synthesis of functionalized bicyclo[3.2.0]heptanes.

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

Reactions of the peroxo intermediate of soluble methane monooxygenase hydroxylase with ethers.

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

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Global Trade Item Number

SKU	GTIN
T6137-1G	04061837358388
PHR3257-500MG	04065267005591
T6137-100MG	04061837358371
T6137-500MG	04061837358395
05010-1L	04061838636058
05010-250ML	04061838636065