A34805
2-烯丙基酚
98%
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线性分子式:
H2C=CHCH2C6H4OH
化学文摘社编号:
分子量:
134.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-119-0
Beilstein/REAXYS Number:
742121
MDL number:
Assay:
98%
Form:
liquid
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
Quality Level
bp
220 °C (lit.)
density
1.028 g/mL at 25 °C (lit.)
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
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
法规信息
新产品
此项目有
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
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
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
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