GF85707513
Palladium
wire reel, 0.5m, diameter 1.0mm, hard, 99.95%
Synonym(s):
Palladium, PD005150
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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
wire
manufacturer/tradename
Goodfellow 857-075-13
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
13 - Non Combustible Solids
wgk_germany
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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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
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
Synthesis of heterocycles via palladium-catalyzed carbonylations.
Xiao-Feng Wu et al.
Chemical reviews, 113(1), 1-35 (2012-10-09)
Update 1 of: Synthesis and functionalization of indoles through palladium-catalyzed reactions.
Sandro Cacchi et al.
Chemical reviews, 111(5), PR215-PR283 (2011-05-12)
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
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