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A35208

Sigma-Aldrich

Allyl phenyl ether

99%

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About This Item

Linear Formula:
C6H5OCH2CH=CH2
CAS Number:
1746-13-0
Molecular Weight:
134.18
Beilstein:
1905622
EC Number:
217-125-3
MDL number:
MFCD00008644
UNSPSC Code:
12162002
PubChem Substance ID:
24890779
NACRES:
NA.23

Assay

99%

form

liquid

refractive index

n20/D 1.522 (lit.)

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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Related Categories

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

145.4 °F - closed cup

Flash Point(C)

63 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF7355
BCCF1620
BCCD5109
BCCB7456
BCBD5611V

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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.
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.
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

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