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Merck
CN

A34805

2-Allylphenol

98%

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About This Item

Linear Formula:
H2C=CHCH2C6H4OH
CAS Number:
1745-81-9
Molecular Weight:
134.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24890775
EC Number:
217-119-0
Beilstein/REAXYS Number:
742121
MDL number:
MFCD00002250

Key Documents

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Product Name

2-Allylphenol, 98%

InChI key

QIRNGVVZBINFMX-UHFFFAOYSA-N

InChI

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

SMILES string

Oc1ccccc1CC=C

assay

98%

form

liquid

refractive index

n20/D 1.546 (lit.)

bp

220 °C (lit.)

density

1.028 g/mL at 25 °C (lit.)

Quality Level

100

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Related Categories

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

flash_point_f

190.4 °F - closed cup

flash_point_c

88 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB4770
STBL0709
STBL0710
STBJ4076
STBJ0459

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Shuangjun Gong et al.
Pest management science, 65(12), 1337-1343 (2009-08-18)
2-Allylphenol is a registered fungicide in China to control fungal diseases on tomato, strawberry and apple. It is synthetic and structurally resembles the active ingredient ginkgol isolated from Ginkgo biloba L. bark. 2-Allylphenol has been used in China for 10
Alvin Kah-wei Hee et al.
Journal of chemical ecology, 30(11), 2127-2138 (2005-01-28)
Pharmacophagy of methyl eugenol (ME)--a highly potent male attractant, by Bactrocera papayae results in the hydroxylation of ME to sex pheromonal components, 2-ally-4,5-dimethoxyphenol (DMP) and (E)-coniferyl alcohol (CF). These compounds, which are also male attractants, are then sequestered and stored
Ji-Ye Hu et al.
Journal of environmental sciences (China), 17(3), 491-493 (2005-08-09)
The method of residue analysis of a new synthesized fungicide 2-allylphenol was studied by simulating the active compound structure in Gingko tree (Gingko biloba L.) and its dissipation rate and terminal residue levels in tomato under field condition. Residues of
Paul Rademacher et al.
Organic & biomolecular chemistry, 3(14), 2620-2625 (2005-07-07)
2-Allylphenol (1) constitutes a mixture of conformers, in which an OH-pi hydrogen bonded closed (1a) and open form (1b) can be distinguished. 4-Substituted 2-allyphenols (2-9) have been synthesised and investigated by theoretical and spectroscopic methods. In 1-9, the energy and
Tianli Qu et al.
Ecotoxicology and environmental safety, 102, 136-141 (2014-02-18)
2-Allylphenol is a biomimetic synthetic fungicide that mimics the compound ginkgol found in gingko fruit (Gingko biloba L.). This systemic fungicide can effectively suppress a wide range of plant diseases, including wheat sharp eyespot (Rhizoctonia cerealis). However, its degradation in
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