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GF35615921

Palladium

Name: Palladium
Brand: ALDRICH

foil, 1m coil, thickness 0.1mm, coil width 2mm, as rolled, 99.95%

Synonyma:

Palladium, PD000276

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen

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About This Item

Lineární vzorec:

Číslo CAS:

7440-05-3

Molekulová hmotnost:

106.42

MDL number:

MFCD00011167

UNSPSC Code:

12141733

PubChem Substance ID:

329805416

NACRES:

NA.23

assay

99.95%

form

foil

manufacturer/tradename

Goodfellow 356-159-21

resistivity

9.96 μΩ-cm, 20°C

L × thickness × width

1 m × 0.1 mm × 2 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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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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Lot/Batch Number

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Recent developments and perspectives in palladium-catalyzed cyanation of aryl halides: synthesis of benzonitriles.

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Chemical Society reviews, 40(10), 5049-5067 (2011-04-30)

The palladium-catalyzed cyanation of Ar-X (X = I, Br, Cl, OTf, and H) allows for an efficient access towards benzonitriles. After its discovery in 1973 and following significant improvements in recent decades, this methodology has become nowadays the most popular

Palladium(II)-catalyzed alkene functionalization via nucleopalladation: stereochemical pathways and enantioselective catalytic applications.

Richard I McDonald et al.

Chemical reviews, 111(4), 2981-3019 (2011-03-25)

Homogeneous palladium-catalyzed asymmetric hydrogenation.

Qing-An Chen et al.

Chemical Society reviews, 42(2), 497-511 (2012-11-10)

The transition metal catalyzed asymmetric hydrogenation of unsaturated compounds arguably presents one of the most attractive methods for the synthesis of chiral compounds. Over the last few decades, Pd has gradually grown up as a new and popular metal catalyst

Palladium-catalyzed oxidative carbonylation reactions.

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Palladium-catalyzed coupling reactions have become a powerful tool for advanced organic synthesis. This type of reaction is of significant value for the preparation of pharmaceuticals, agrochemicals, as well as advanced materials. Both, academic as well as industrial laboratories continuously investigate

Progress in palladium-based catalytic systems for the sustainable synthesis of annulated heterocycles: a focus on indole backbones.

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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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