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P49805

Sigma-Aldrich

Piperonylic acid

99%

Sinónimos:

1,3-Benzodioxole-5-carboxylic acid, 3,4-(Methylenedioxy)benzoic acid

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About This Item

Fórmula empírica (notación de Hill):
C8H6O4
Número de CAS:
94-53-1
Peso molecular:
166.13
Beilstein/REAXYS Number:
150206
EC Number:
202-342-8
MDL number:
MFCD00005830
UNSPSC Code:
12352100
PubChem Substance ID:
24898575
NACRES:
NA.22

assay

99%

form

powder

mp

229-231 °C (lit.)

SMILES string

OC(=O)c1ccc2OCOc2c1

InChI

1S/C8H6O4/c9-8(10)5-1-2-6-7(3-5)12-4-11-6/h1-3H,4H2,(H,9,10)

InChI key

VDVJGIYXDVPQLP-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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R Ranga Rao et al.
Bioorganic & medicinal chemistry, 17(14), 5170-5175 (2009-06-12)
A bioassay-guided fractionation and chemical examination of antihyperglycemic root extract of Derris indica resulted in isolation and characterization of two new furanoflavanoids (1, 2) along with thirteen known compounds (3-15). Their structures were determined on the basis of extensive spectroscopic
Eyal Shimoni et al.
Journal of biotechnology, 105(1-2), 61-70 (2003-09-27)
Propenylbenzenes are often used as starting materials in the chemical synthesis of aroma compounds and fine chemicals. In the present study, we demonstrate the ability of an Arthrobacter sp. to transform various structures of propenylbenzenes derived from essential oils to
Gisele Adriana Bubna et al.
Journal of plant physiology, 168(14), 1627-1633 (2011-04-15)
The allelopathic effect of caffeic acid was tested on root growth, phenylalanine ammonia-lyase (PAL) and peroxidase (POD) activities, hydrogen peroxide (H(2)O(2)) accumulation, lignin content and monomeric composition of soybean (Glycine max) roots. We found that exogenously applied caffeic acid inhibited
Debabrata Sircar et al.
Journal of plant physiology, 166(13), 1370-1380 (2009-04-04)
Biosynthesis of hydroxybenzoates even at enzymatic level is poorly understood. In this report, effect of feeding of putative biosynthetic precursors and pathway-specific enzyme inhibitors of early phenylpropanoid pathway on p-hydroxybenzoic acid accumulation in chitosan-elicited hairy roots of Daucus carota was
Guillaume A Schoch et al.
Plant physiology, 130(2), 1022-1031 (2002-10-12)
The cinnamate (CA) 4-hydroxylase (C4H) is a cytochrome P450 that catalyzes the second step of the main phenylpropanoid pathway, leading to the synthesis of lignin, pigments, and many defense molecules. Salicylic acid (SA) is an essential trigger of plant disease
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