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About This Item
Linear Formula:
C6H5OCH2CH=CH2
CAS Number:
Molecular Weight:
134.18
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
217-125-3
Beilstein/REAXYS Number:
1905622
MDL number:
Quality Level
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
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
145.4 °F - closed cup
flash_point_c
63 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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
| SKU | GTIN |
|---|---|
| A35208-25G | 04061833467046 |