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GF94632576

Palladium

foil, light tested, 100x100mm, thickness 0.075mm, as rolled, 99.95%

Sinônimo(s):

Palladium, PD000272

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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:
329814247
NACRES:
NA.23

Ensaio

≥99.95%

Formulário

foil

fabricante/nome comercial

Goodfellow 946-325-76

resistividade

9.96 μΩ-cm, 20°C

p.e.

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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Lot/Batch Number

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Synthesis of heterocycles via palladium-catalyzed carbonylations.
Xiao-Feng Wu et al.
Chemical reviews, 113(1), 1-35 (2012-10-09)
Anton V Dubrovskiy et al.
Combinatorial chemistry & high throughput screening, 15(6), 451-472 (2012-01-26)
The iodocyclization of functionally-substituted alkynes provides an excellent way to prepare a wide range of iodoheterocycles, which can then be readily elaborated through palladium-catalyzed Suzuki-Miyaura, Sonogashira, Heck, Hartwig-Buchwald, and carbonylation processes into libraries of medicinally relevant heterocycles. The synthesis of
Keary M Engle et al.
The Journal of organic chemistry, 78(18), 8927-8955 (2013-04-10)
Homogeneous transition-metal-catalyzed reactions are indispensable to all facets of modern chemical synthesis. It is thus difficult to imagine that for much of the early 20th century, the reactivity and selectivity of all known homogeneous metal catalysts paled in comparison to
Masahiro Toyota
Natural product communications, 8(7), 999-1004 (2013-08-29)
A novel palladium-catalyzed intramolecular oxidative alkylation of unactivated olefins is described. This protocol was devised to solve one of the drawbacks of the original palladium-catalyzed cycloalkenylation that we developed. We call this new procedure the 'second generation palladium-catalyzed cycloalkenylation'. This
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
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