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About This Item
Linear Formula:
C6H5OCH2CH=CH2
CAS Number:
Molecular Weight:
134.18
Beilstein:
1905622
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
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
Certificates of Analysis (COA)
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[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.
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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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