P49406
Piperonyl alcohol
98%
Sinónimos:
1,3-Benzodioxole-5-methanol, 3,4-(Methylenedioxy)benzyl alcohol, 3,4-(Methylenedioxy)phenylmethanol
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About This Item
Fórmula empírica (notación de Hill):
C8H8O3
Número de CAS:
Peso molecular:
152.15
Beilstein/REAXYS Number:
136113
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
98%
form
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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Categorías relacionadas
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Daniel Schwendenwein et al.
Advanced synthesis & catalysis, 358(21), 3414-3421 (2016-12-06)
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
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
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
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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