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GF34072815

Palladium

rod, 25mm, diameter 4.0mm, 99.95%

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Synonym(s):
Palladium, PD007940
Linear Formula:
Pd
CAS Number:
Molecular Weight:
106.42
MDL number:
PubChem Substance ID:
NACRES:
NA.23

assay

99.95%

form

rod

manufacturer/tradename

Goodfellow 340-728-15

resistivity

9.96 μΩ-cm, 20°C

L × diam.

25 mm × 4.0 mm

bp

2970 °C (lit.)

mp

1554 °C (lit.)

density

12.02 g/cm3 (lit.)

SMILES string

[Pd]

InChI

1S/Pd

InChI key

KDLHZDBZIXYQEI-UHFFFAOYSA-N

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1 of 4

This Item
GF19845120GF81435146GF89451489
Palladium rod, 25mm, diameter 4.0mm, 99.95%

GF34072815

Palladium

Palladium rod, 50mm, diameter 4.0mm, 99.95%

GF19845120

Palladium

Palladium rod, 100mm, diameter 2.0mm, 99.95%

GF81435146

Palladium

Palladium rod, 50mm, diameter 2.0mm, 99.95%

GF89451489

Palladium

assay

99.95%

assay

99.95%

assay

99.95%

assay

≥99.95%

manufacturer/tradename

Goodfellow 340-728-15

manufacturer/tradename

Goodfellow 198-451-20

manufacturer/tradename

Goodfellow 814-351-46

manufacturer/tradename

Goodfellow 894-514-89

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

bp

2970 °C (lit.)

bp

2970 °C (lit.)

bp

2970 °C (lit.)

bp

2970 °C (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

General description

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

Legal Information

Product of Goodfellow

Storage Class

13 - Non Combustible Solids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_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
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
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
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
Update 1 of: Synthesis and functionalization of indoles through palladium-catalyzed reactions.
Sandro Cacchi et al.
Chemical reviews, 111(5), PR215-PR283 (2011-05-12)

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