P49805
Piperonylic acid
99%
Sinónimos:
1,3-Benzodioxole-5-carboxylic acid, 3,4-(Methylenedioxy)benzoic acid
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Fórmula empírica (notación de Hill):
C8H6O4
Número CAS:
Peso molecular:
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
Servicio técnico
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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
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
Yue Zhu et al.
Journal of the American Chemical Society, 128(13), 4267-4276 (2006-03-30)
Two-photon excitation (2PE) of "caged" biomolecules represents a powerful method to investigate the temporal and spatial relevance of physiological function in real time and on living tissue, because the excitation volume can be restricted to 1 fL. Additionally, low-energy IR