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MilliporeSigma

A35208

Allyl phenyl ether

99%

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25 G

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$152.15

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About This Item

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

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Product Name

Allyl phenyl ether, 99%

InChI key

POSICDHOUBKJKP-UHFFFAOYSA-N

InChI

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

SMILES string

C=CCOc1ccccc1

assay

99%

form

liquid

refractive index

n20/D 1.522 (lit.)

bp

192 °C (lit.)

density

0.978 g/mL at 25 °C (lit.)

Quality Level

200

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This Item
298964139548185248
Allyl phenyl ether 99%

Sigma-Aldrich

A35208

Allyl phenyl ether

N,N′-Diisopropylethylenediamine 99%

Sigma-Aldrich

298964

N,N′-Diisopropylethylenediamine

Di(ethylene glycol) divinyl ether 99%

Sigma-Aldrich

139548

Di(ethylene glycol) divinyl ether

Allyl acetate 99%

Sigma-Aldrich

185248

Allyl acetate

assay

99%

assay

99%

assay

99%

assay

99%

density

0.978 g/mL at 25 °C (lit.)

density

0.798 g/mL at 25 °C (lit.)

density

0.968 g/mL at 25 °C (lit.)

density

0.928 g/mL at 25 °C (lit.)

bp

192 °C (lit.)

bp

169-171 °C (lit.)

bp

198-199 °C (lit.)

bp

103-104 °C (lit.)

refractive index

n20/D 1.522 (lit.)

refractive index

n20/D 1.4289 (lit.)

refractive index

n20/D 1.446 (lit.)

refractive index

n20/D 1.404 (lit.)

form

liquid

form

-

form

-

form

liquid

Quality Level

200

Quality Level

-

Quality Level

100

Quality Level

100

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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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6241
SDBB2951
STBL1483
BCCF7355
BCCF1620

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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

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