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Key Documents

GF35373551

Palladium

foil, 10x10mm, thickness 0.50mm, as rolled, 99.99+%

Sinonimo/i:

Palladium, PD000351

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About This Item

Formula condensata:
Pd
Numero CAS:
Peso molecolare:
106.42
Numero MDL:
Codice UNSPSC:
12141733
ID PubChem:
NACRES:
NA.23

Saggio

99.99%

Forma fisica

foil

Produttore/marchio commerciale

Goodfellow 353-735-51

Resistività

9.96 μΩ-cm, 20°C

Misura × spessore

10x10 mm × 0.50 mm

P. eboll.

2970 °C (lit.)

Punto di fusione

1554 °C (lit.)

Densità

12.02 g/cm3 (lit.)

Stringa SMILE

[Pd]

InChI

1S/Pd
KDLHZDBZIXYQEI-UHFFFAOYSA-N

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Descrizione generale

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

Note legali

Product of Goodfellow

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

nwg

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Pazhamalai Anbarasan et al.
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
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(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)
Xiao-Feng Wu et al.
ChemSusChem, 6(2), 229-241 (2013-01-12)
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
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

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