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GF06612847

Palladium

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

Sinónimos:

Palladium, PD000276

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About This Item

Fórmula lineal:
Pd
Número de CAS:
7440-05-3
Peso molecular:
106.42
MDL number:
MFCD00011167
UNSPSC Code:
12141733
PubChem Substance ID:
329801071
NACRES:
NA.23

assay

99.95%

form

foil

manufacturer/tradename

Goodfellow 066-128-47

resistivity

9.96 μΩ-cm, 20°C

L × thickness × W

0.1 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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Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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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