GF43081174
Palladium
foil, not light tested, 100x100mm, thickness 0.0125mm, 99.95%
Synonym(s):
Palladium, PD000250
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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
Pricing and availability is not currently available.
Assay
99.95%
form
foil
manufacturer/tradename
Goodfellow 430-811-74
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.
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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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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
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)
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
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
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
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