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Merck
모든 사진(2)

주요 문서

P49805

Sigma-Aldrich

Piperonylic acid

99%

동의어(들):

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

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About This Item

실험식(Hill 표기법):
C8H6O4
CAS Number:
Molecular Weight:
166.13
Beilstein:
150206
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

99%

양식

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 Code

11 - Combustible Solids

WGK

WGK 3

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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
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
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
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
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

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