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GF90054659

Palladium

rod, 50mm, diameter 6.0mm, 99.95%

Synonym(e):

Palladium, PD007950

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About This Item

Lineare Formel:
Pd
CAS-Nummer:
7440-05-3
Molekulargewicht:
106.42
MDL-Nummer:
MFCD00011167
UNSPSC-Code:
12141733
PubChem Substanz-ID:
329813563
NACRES:
NA.23

Assay

≥99.95%

Form

rod

Hersteller/Markenname

Goodfellow 900-546-59

Widerstandsfähigkeit

9.96 μΩ-cm, 20°C

bp

2970 °C (lit.)

mp (Schmelzpunkt)

1554 °C (lit.)

Dichte

12.02 g/cm3 (lit.)

SMILES String

[Pd]

InChI

1S/Pd

InChIKey

KDLHZDBZIXYQEI-UHFFFAOYSA-N

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Allgemeine Beschreibung

For updated SDS information please visit www.goodfellow.com.

Rechtliche Hinweise

Product of Goodfellow

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

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Lot/Batch Number

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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
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
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