GF65258703
Palladium
foil, 4mm disks, thickness 0.03mm, as rolled, 99.95%
Synonym(s):
Palladium, PD000261
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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
Assay
99.95%
form
foil
manufacturer/tradename
Goodfellow 652-587-03
resistivity
9.96 μΩ-cm, 20°C
diam. × thickness
4 mm × 0.03 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.
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Product of Goodfellow
Storage Class Code
13 - Non Combustible Solids
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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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
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
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
Keary M Engle et al.
The Journal of organic chemistry, 78(18), 8927-8955 (2013-04-10)
Homogeneous transition-metal-catalyzed reactions are indispensable to all facets of modern chemical synthesis. It is thus difficult to imagine that for much of the early 20th century, the reactivity and selectivity of all known homogeneous metal catalysts paled in comparison to
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
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