GF44874995
Palladium
foil, light tested, 100x100mm, thickness 0.047mm, as rolled, 99.95%
Synonym(s):
Palladium, PD000262
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About This Item
Linear Formula:
Pd
CAS Number:
Molecular Weight:
106.42
MDL number:
UNSPSC Code:
12141733
PubChem Substance ID:
NACRES:
NA.23
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Assay
99.95%
form
foil
manufacturer/tradename
Goodfellow 448-749-95
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 Code
13 - Non Combustible Solids
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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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
Simon De Corte et al.
Microbial biotechnology, 5(1), 5-17 (2011-05-11)
While precious metals are available to a very limited extent, there is an increasing demand to use them as catalyst. This is also true for palladium (Pd) catalysts and their sustainable recycling and production are required. Since Pd catalysts exist
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
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
Mélanie Platon et al.
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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