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GF75251909

Palladium

microfoil, disks, 10mm, thinness 0.05μm, specific density 63.6μg/cm2, permanent mylar 3.5μm support, 99.99%

Sinônimo(s):

Palladium, PD004300

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About This Item

Fórmula linear:
Pd
Número CAS:
7440-05-3
Peso molecular:
106.42
Número MDL:
MFCD00011167
Código UNSPSC:
12141733
ID de substância PubChem:
329811266
NACRES:
NA.23

Ensaio

99.99%

forma

foil

fabricante/nome comercial

Goodfellow 752-519-09

resistividade

9.96 μΩ-cm, 20°C

diâmetro × espessura

10 mm × 0.05 μm

pb

2970 °C (lit.)

pf

1554 °C (lit.)

densidade

12.02 g/cm3 (lit.)

cadeia de caracteres SMILES

[Pd]

InChI

1S/Pd

chave InChI

KDLHZDBZIXYQEI-UHFFFAOYSA-N

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Descrição geral

For updated SDS information please visit www.goodfellow.com.

Informações legais

Product of Goodfellow

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

nwg

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Jana Doháňošová et al.
Molecules (Basel, Switzerland), 18(6), 6173-6192 (2013-05-28)
The palladium (II)-catalysed reactions of alkenols and aminoalkenols such as oxycarbonylations or bicyclisations are powerful methods for the construction of oxygen and nitrogen-containing heterocyclic compounds. This review highlights recent progress in the development of the asymmetric palladium(II)-catalysed Wacker-type cyclisations of
Simon De Corte et al.
Microbial biotechnology, 5(1), 5-17 (2011-05-11)
While precious metals are available to a very limited extent, there is an increasing demand to use them as catalyst. This is also true for palladium (Pd) catalysts and their sustainable recycling and production are required. Since Pd catalysts exist
M Angeles Fernández-Ibañez et al.
Molecules (Basel, Switzerland), 18(9), 10108-10121 (2013-08-27)
The dual activation of simple substrates by the combination of organocatalysis and palladium catalysis has been successfully applied in a variety of different asymmetric transformations. Thus, the asymmetric a-allylation of carbonyl compounds, a-fluorination of acyl derivatives, decarboxylative protonation of β-dicarbonyl
Masahiro Yoshida
Chemical & pharmaceutical bulletin, 60(3), 285-299 (2012-03-03)
It is known that propargylic compounds having an ester and a halide at the propargylic positions react with palladium complexes leading to π-propargylpalladium and allenylpalladium complexes, which cause various transformations in the presence of the reactants. The aim of the
Mélanie Platon et al.
Chemical Society reviews, 41(10), 3929-3968 (2012-03-27)
A survey highlighting the most recent palladium catalytic systems produced and their performances for progress in direct synthesis of indole backbones by heterocarbocyclization of reactive substrates is provided. The discussion is developed in relation with the principles of sustainable chemistry
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