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A34805

Sigma-Aldrich

2-Allylphenol

98%

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About This Item

Formula condensata:
H2C=CHCH2C6H4OH
Numero CAS:
1745-81-9
Peso molecolare:
134.18
Beilstein:
742121
Numero CE:
217-119-0
Numero MDL:
MFCD00002250
Codice UNSPSC:
12352100
ID PubChem:
24890775
NACRES:
NA.22

Saggio

98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.546 (lit.)

P. eboll.

220 °C (lit.)

Densità

1.028 g/mL at 25 °C (lit.)

Stringa SMILE

Oc1ccccc1CC=C

InChI

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

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Pittogrammi

Skull and crossbonesCorrosion
GHS06,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311,H314

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

190.4 °F - closed cup

Punto d’infiammabilità (°C)

88 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
STBJ4076
STBJ0459
STBH6558
STBH4867
STBH4866

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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
Meyyappan Arumugam et al.
Applied microbiology and biotechnology, 86(1), 109-117 (2009-11-11)
A marine actinobacterium isolated from the Bay of Bengal, India and previously found to be producing an antimicrobial and cytotoxic terpenoid was further investigated for antimicrobial metabolites. The bacterium was preliminarily identified as a new species of the genus Streptomyces
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
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