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About This Item
Linear Formula:
Pd
CAS Number:
Molecular Weight:
106.42
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12141733
MDL number:
InChI
1S/Pd
SMILES string
[Pd]
InChI key
KDLHZDBZIXYQEI-UHFFFAOYSA-N
assay
99.95%
form
foil
manufacturer/tradename
Goodfellow 038-288-32
resistivity
9.96 μΩ-cm, 20°C
diam. × thickness
15 mm × 0.125 mm
bp
2970 °C (lit.)
mp
1554 °C (lit.)
density
12.02 g/cm3 (lit.)
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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
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
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Amanda J Hickman et al.
Nature, 484(7393), 177-185 (2012-04-14)
Copper and palladium catalysts are critically important in numerous commercial chemical processes. Improvements in the activity, selectivity and scope of these catalysts could drastically reduce the environmental impact, and increase the sustainability, of chemical reactions. One rapidly developing strategy for
Synthesis of heterocycles via palladium-catalyzed carbonylations.
Xiao-Feng Wu et al.
Chemical reviews, 113(1), 1-35 (2012-10-09)
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
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
Anton V Dubrovskiy et al.
Combinatorial chemistry & high throughput screening, 15(6), 451-472 (2012-01-26)
The iodocyclization of functionally-substituted alkynes provides an excellent way to prepare a wide range of iodoheterocycles, which can then be readily elaborated through palladium-catalyzed Suzuki-Miyaura, Sonogashira, Heck, Hartwig-Buchwald, and carbonylation processes into libraries of medicinally relevant heterocycles. The synthesis of
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