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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:
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
| SKU | GTIN |
|---|---|
| 8086149025 | 04022536873145 |
| M2659-100G | 04061834045915 |
| M2659-3KG | 04061833553824 |
| 52549-250MG | 04061832552040 |
| 1379183-250MG | 04061838732095 |
| 8086141000 | 04022536401034 |
| 8086140100 | 04022536401027 |
| M2659-5G | 04061835559541 |
| PHR1274-1G | 04061835233373 |
| BP1295 | 04065270231161 |
| M2659-1KG | 04061835559534 |