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GF43081174

Palladium

Name: Palladium
Brand: ALDRICH

foil, not light tested, 100x100mm, thickness 0.0125mm, 99.95%

Sinónimos:

Palladium, PD000250

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About This Item

Fórmula lineal:

Número de CAS:

7440-05-3

Peso molecular:

106.42

MDL number:

MFCD00011167

UNSPSC Code:

12141733

PubChem Substance ID:

329806578

NACRES:

NA.23

assay

99.95%

form

foil

manufacturer/tradename

Goodfellow 430-811-74

resistivity

9.96 μΩ-cm, 20°C

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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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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High-valent organometallic copper and palladium in catalysis.

Amanda J Hickman et al.

Nature, 484(7393), 177-185 (2012-04-14)

Copper and palladium catalysts are critically important in numerous commercial chemical processes. Improvements in the activity, selectivity and scope of these catalysts could drastically reduce the environmental impact, and increase the sustainability, of chemical reactions. One rapidly developing strategy for

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)

Synthesis of heterocycles via palladium-catalyzed carbonylations.

Xiao-Feng Wu et al.

Chemical reviews, 113(1), 1-35 (2012-10-09)

Asymmetric palladium-catalysed intramolecular Wacker-type cyclisations of unsaturated alcohols and amino alcohols.

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

Development of a second generation palladium-catalyzed cycloalkenylation and its application to bioactive natural product synthesis.

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

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