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文件

安全信息

P49406

Sigma-Aldrich

胡椒醇

98%

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别名:
3,4-亚甲二氧基苯甲醇, 3,4-亚甲二氧苄醇, 5-羟甲基苯并-1,3-二噁环戊烷
经验公式（希尔记法）:
C8H8O3
CAS号:
495-76-1
分子量:
152.15
Beilstein:
136113
EC 号:
207-808-4
MDL编号:
MFCD00005836
PubChem化学物质编号:
24898572
NACRES:
NA.22

检测方案

98%

形式

solid

mp

50-54 °C (lit.)

SMILES string

OCc1ccc2OCOc2c1

InChI

1S/C8H8O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-3,9H,4-5H2

InChI key

BHUIUXNAPJIDOG-UHFFFAOYSA-N

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相关类别

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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Daniel Schwendenwein et al.
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The enzymatic reduction of carboxylic acids is in its infancy with only a handful of biocatalysts available to this end. We have increased the spectrum of carboxylate-reducing enzymes (CARs) with the sequence of a fungal CAR from Neurospora crassa OR74A
S R Victor et al.
Pest management science, 57(7), 603-608 (2001-07-24)
The development of Leucoagaricus gongylophorus, the fungus cultured by the leaf-cutting ant Atta sexdens was inhibited in vitro by synthetic compounds containing the piperonyl group. In addition, worker ants that were fed daily on an artificial diet to which these
Marise M O Cabral et al.
Fitoterapia, 79(1), 59-63 (2007-10-02)
The neolignan, burchellin, a natural compound that reduces urine excretion in larvae of the bloodsucking bug, Rhodnius prolixus, a vector of Chagas' disease, is rapidly degraded in the hemolymph of the insect. The main product that accumulates in this tissue
Metabolism of piperonal and piperonyl alcohol in the rat with special reference to the scission of the methylenedioxy group.
J Klungsøyr et al.
Acta pharmaceutica Suecica, 21(1), 67-72 (1984-01-01)
Aaron D Gross et al.
Chemico-biological interactions, 263, 1-6 (2016-12-18)
An outbreak of the southern cattle tick, Rhipicephalus (Boophilus) microplus, (Canestrini), in the United States would have devastating consequences on the cattle industry. Tick populations have developed resistance to current acaricides, highlighting the need to identify new biochemical targets along
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