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A34805

Sigma-Aldrich

2-Allylphenol

98%

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About This Item

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

Assay

98%

form

liquid

refractive index

n20/D 1.546 (lit.)

bp

220 °C (lit.)

density

1.028 g/mL at 25 °C (lit.)

SMILES string

Oc1ccccc1CC=C

InChI

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

InChI key

QIRNGVVZBINFMX-UHFFFAOYSA-N

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Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301 + H311,H314

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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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