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Palladium
foil, thickness 0.025 mm, 99.9% trace metals basis
Synonym(e):
Palladium (powder), Palladium black, Palladium element
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190 MG
€ 180,00
About This Item
Lineare Formel:
Pd
CAS-Nummer:
Molekulargewicht:
106.42
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12141733
PubChem Substanz-ID:
NACRES:
NA.23
Empfohlene Produkte
Qualitätsniveau
Assay
99.9% trace metals basis
Form
foil
Widerstandsfähigkeit
9.96 μΩ-cm, 20°C
Dicke
0.025 mm
bp
2970 °C (lit.)
mp (Schmelzpunkt)
1554 °C (lit.)
Dichte
12.02 g/cm3 (lit.)
SMILES String
[Pd]
InChI
1S/Pd
InChIKey
KDLHZDBZIXYQEI-UHFFFAOYSA-N
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Lagerklassenschlüssel
13 - Non Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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As novel therapeutic agents relevant to colon cancer therapy are explored continuously, we tested 4 R2edda-type ligand precursors O,O'-dialkyl esters of (S,S)-ethylenediamine-N,N'-di-2-(4-methyl)pentanoic acid (L1.2HCl-L4.2HCl) and corresponding palladium(II) and platinum(II) complexes against the human colon cancer cell lines CaCo-2, SW480 and
Daniel Smykowski et al.
Journal of molecular graphics & modelling, 41, 89-96 (2013-03-21)
This study is the analysis of the adsorption process of the CO2 molecule on the cationic sites of the DOH zeolite. Based on the DFT method, we have been able to identify several adsorption sites containing extra-framework cations and evaluate
Gary A Molander et al.
The Journal of organic chemistry, 78(8), 4123-4131 (2013-04-11)
A method has been developed for the Pd-catalyzed synthesis of α-(hetero)aryl esters and amides through a Suzuki-Miyaura cross-coupling reaction. This method avoids the use of strong base, does not necessitate inert or low temperature formation of reagents, and does not
Xuxing Chen et al.
Organic & biomolecular chemistry, 11(16), 2582-2585 (2013-03-19)
A one-pot two-step synthesis of versatile indenones has been developed. This palladium(II)-catalyzed transformation involves generation and condensation of ortho-functionalized 1,2-benzils from 2-(2-arylethynylphenyl)acetonitriles using Ph2SO as the oxidant. The resulting 3-cyanoindenones can be converted to various valuable molecules.
Meifang Zheng et al.
Organic letters, 15(8), 1838-1841 (2013-04-02)
Palladium-catalyzed oxidative difunctionalization of enol ethers with 1,3-dicarbonyl compounds to construct trisubstituted furans in one step under mild conditions is described. The reaction is thought to proceed through a C-C bond formation along with a C-O bond closing the ring
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