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771902

Sigma-Aldrich

Phenyl vinyl ether

97%

Sinónimos:

(Ethenyloxy)benzene, Phenoxyethylene

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About This Item

Fórmula empírica (notación de Hill):
C8H8O
Número de CAS:
766-94-9
Peso molecular:
120.15
MDL number:
MFCD00081208
UNSPSC Code:
12352100
PubChem Substance ID:
329767525
NACRES:
NA.22

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.522 (lit.)

density

0.978 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C=COc1ccccc1

InChI

1S/C8H8O/c1-2-9-8-6-4-3-5-7-8/h2-7H,1H2

InChI key

NHOGGUYTANYCGQ-UHFFFAOYSA-N

Categorías relacionadas

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Sens. 1

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

60.8 °F

flash_point_c

16 °C

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Hee-Kwon Kim et al.
ACS applied materials & interfaces, 5(12), 5648-5658 (2013-06-19)
Novel pH-responsive assemblies (PEG-lipid:DOPE liposomes) containing tunable and bifunctional phenyl-substituted vinyl ether (PIVE) cross-linkers were prepared. The assemblies consisted of 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), acid-cleavable poly(ethylene glycol) (PEG)-conjugated lipids, pDNA, and protamine sulfate (PS). The PIVE linkage was designed to hydrolyze under
Shihua Wang et al.
Organic letters, 13(22), 5968-5971 (2011-10-20)
Benzo[b]furans were prepared in one pot based on the addition/palladium-catalyzed C-H bond functionalization of phenols with bromoalkynes. The addition reactions of phenols to bromoalkynes generated (Z)-2-bromovinyl phenyl ethers in high yields with excellent regio- and stereoselectivity. The obtained (Z)-2-bromovinyl phenyl
M Isobe et al.
The Journal of toxicological sciences, 20(2), 161-164 (1995-05-01)
4-Nitrophenyl vinyl ether (NPVE) and phenyl vinyl ether (PVE) administered i.p. in mice lowered hepatic non-protein sulfhydryl (NP-SH) content, but did not elevate the serum glutamate pyruvate transaminase (GPT) activity. n-Butyl vinyl ether (BVE) showed no significant effects either on
Christopher L Rock et al.
Dalton transactions (Cambridge, England : 2003), 48(2), 461-467 (2018-11-30)
The phosphine-substituted α-diimine Ni precursor, (Ph2PPrDI)Ni, has been found to catalyze alkene hydrosilylation in the presence of Ph2SiH2 with turnover frequencies of up to 124 h-1 at 25 °C (990 h-1 at 60 °C). Moreover, the selective hydrosilylation of allylic

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