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Merck
CN

06055

Allyl phenyl ether

puriss., ≥98.5% (GC)

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About This Item

Linear Formula:
C6H5OCH2CH=CH2
CAS Number:
Molecular Weight:
134.18
EC Number:
217-125-3
UNSPSC Code:
12162002
PubChem Substance ID:
Beilstein/REAXYS Number:
1905622
MDL number:
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grade

puriss.

assay

≥98.5% (GC)

refractive index

n20/D 1.522

bp

192 °C (lit.)

density

0.978 g/mL at 25 °C (lit.)

SMILES string

C=CCOc1ccccc1

InChI

1S/C9H10O/c1-2-8-10-9-6-4-3-5-7-9/h2-7H,1,8H2

InChI key

POSICDHOUBKJKP-UHFFFAOYSA-N



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Ralph Moser et al.
Organic letters, 12(1), 28-31 (2009-12-03)
Allylic phenyl ethers serve as electrophiles toward Pd(0) en route to a variety of allylic silanes. The reactions can be run at room temperature in water as the only medium using micellar catalysis.
Anders Dahlén et al.
Organic letters, 5(22), 4085-4088 (2003-10-24)
[reaction: see text]. SmI2/H2O/amine provides selective cleavage of unsubstituted allyl ethers in good to excellent yields. This method is therefore useful in deprotection of alcohols and carbohydrates.
M Mahmoudian et al.
Applied microbiology and biotechnology, 37(1), 28-31 (1992-04-01)
Eighteen newly isolated ethene- and propene-utilizing bacteria were screened for the ability to produce phenyl glycidyl ether, a common precursor for the synthesis of beta blockers, from phenyl allyl ether. These organisms included Aerococcus, Alcaligenes, Micrococcus and Staphylococcus spp. and



Global Trade Item Number

SKUGTIN
808614902504022536873145
M2659-100G04061834045915
M2659-3KG04061833553824
52549-250MG04061832552040
1379183-250MG04061838732095
808614100004022536401034
808614010004022536401027
M2659-5G04061835559541
PHR1274-1G04061835233373
BP129504065270231161
M2659-1KG04061835559534