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32430

Supelco

Cafenstrole

PESTANAL®, analytical standard

Sinônimo(s):

N,N-Diethyl-3-mesitylsulfonyl-1H-1,2,4-triazole-1-carboxamide

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About This Item

Fórmula empírica (Notação de Hill):
C16H22N4O3S
Número CAS:
125306-83-4
Peso molecular:
350.44
Beilstein:
8432754
Número MDL:
MFCD01631150
Código UNSPSC:
41116107
ID de substância PubChem:
329754206

grau

analytical standard

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

agriculture
environmental

Formato

neat

cadeia de caracteres SMILES

CCN(CC)C(=O)n1cnc(n1)S(=O)(=O)c2c(C)cc(C)cc2C

InChI

1S/C16H22N4O3S/c1-6-19(7-2)16(21)20-10-17-15(18-20)24(22,23)14-12(4)8-11(3)9-13(14)5/h8-10H,6-7H2,1-5H3

chave InChI

HFEJHAAIJZXXRE-UHFFFAOYSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informações legais

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Certificados de análise (COA)

Lot/Batch Number

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Yanming Ma et al.
Journal of agricultural and food chemistry, 54(20), 7724-7728 (2006-09-28)
Based on the carbamoyl triazole herbicide Cafenstrole, 12 novel selenium-containing compounds were designed and synthesized. All of the compounds were characterized and confirmed by IR, 1H NMR, and high-resolution mass spectroscopy. The bioassay tests showed that some of the compounds
A M Abd El-Aty et al.
Biomedical chromatography : BMC, 22(3), 306-315 (2007-12-07)
The present work reports the extraction and clean-up procedures, as well as the chromatographic conditions developed, for the determination of cafenstrole and its metabolite (CHM-03) residues in brown rice grains and rice straw using HPLC-UV detection. The method makes use
Takashi Nobusawa et al.
Genes to cells : devoted to molecular & cellular mechanisms, 17(8), 709-719 (2012-06-28)
Recent studies have showed the essential mechanisms for plastid division that have bacterial orthologues, such as FtsZ and Min system proteins; however, causal factors regulating plastid division in plant cells are poorly understood. Here, we show that plastid division is
Heather D VanGuilder Starkey et al.
The European journal of neuroscience, 37(10), 1643-1658 (2013-02-27)
Myelin-associated inhibitor/NgR1 signaling has important roles in modulation of synaptic plasticity, with demonstrated effects on cognitive function. We have previously demonstrated that NgR1 and its ligands are upregulated in the hippocampus of aged rats with impaired spatial learning and memory
H Takahashi et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 56(9-10), 781-786 (2001-11-29)
The rice herbicide cafenstrole and its analogs inhibited the incorporation of [1-(14)C]-oleate and (2-(14)C]-malonate into very-long-chain fatty acids (VLCFAs), using Scenedesmus cells and leek microsomes from Allium porrum. Although the precise mode of interaction of cafenstrole at the molecular level
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