P49805
Piperonylic acid
99%
Synonym(s):
1,3-Benzodioxole-5-carboxylic acid, 3,4-(Methylenedioxy)benzoic acid
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About This Item
Empirical Formula (Hill Notation):
C8H6O4
CAS Number:
Molecular Weight:
166.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-342-8
Beilstein/REAXYS Number:
150206
MDL number:
Assay:
99%
Form:
powder
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
Storage Class
11 - Combustible Solids
wgk
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
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
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