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GF60234533

Palladium

foil, 8mm disks, thickness 0.25mm, as rolled, 99.99+%

Synonym(s):

Palladium, PD000310

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About This Item

Linear Formula:
Pd
CAS Number:
7440-05-3
Molecular Weight:
106.42
MDL number:
MFCD00011167
UNSPSC Code:
12141733
PubChem Substance ID:
329809086
NACRES:
NA.23

Assay

99.99%

form

foil

manufacturer/tradename

Goodfellow 602-345-33

resistivity

9.96 μΩ-cm, 20°C

diam. × thickness

8 mm × 0.25 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.

Legal Information

Product of Goodfellow

Storage Class Code

13 - Non Combustible Solids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

GF60234533-20EA:
GF60234533-10EA:

Certificates of Analysis (COA)

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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
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
Synthesis of heterocycles via palladium-catalyzed carbonylations.
Xiao-Feng Wu et al.
Chemical reviews, 113(1), 1-35 (2012-10-09)
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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