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GF36099311

Palladium

wire reel, 10m, diameter 0.25mm, hard, 99.95%

Synonym(s):

Palladium, PD005130

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1 EA
HUF 790,000.00

HUF 790,000.00

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1 EA
HUF 790,000.00

About This Item

Linear Formula:
Pd
CAS Number:
7440-05-3
Molecular Weight:
106.42
MDL number:
MFCD00011167
UNSPSC Code:
12141733
PubChem Substance ID:
329805501
NACRES:
NA.23

HUF 790,000.00

Usually ships in 1 week. (Orders outside of US and Europe, please allow an additional 1-2 weeks for delivery)
Request a Bulk Order

Assay

99.95%

form

wire

manufacturer/tradename

Goodfellow 360-993-11

resistivity

9.96 μΩ-cm, 20°C

L × diam.

10 m × 0.25 mm

bp

2970 °C (lit.)

mp

1554 °C (lit.)

density

12.02 g/cm3 (lit.)

SMILES string

[Pd]

InChI

1S/Pd

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This Item
GF40398352GF24288790GF61398197
Palladium wire reel, 10m, diameter 0.25mm, hard, 99.95%

GF36099311

Palladium

Palladium wire reel, 1m, diameter 0.25mm, hard, 99.95%

GF40398352

Palladium

Palladium wire reel, 5m, diameter 0.25mm, hard, 99.95%

GF24288790

Palladium

Palladium wire reel, 0.05m, diameter 1.0mm, hard, 99.95%

GF61398197

Palladium

assay

99.95%

assay

99.95%

assay

99.95%

assay

99.95%

manufacturer/tradename

Goodfellow 360-993-11

manufacturer/tradename

Goodfellow 403-983-52

manufacturer/tradename

Goodfellow 242-887-90

manufacturer/tradename

Goodfellow 613-981-97

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

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

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    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
    Simon De Corte et al.
    Microbial biotechnology, 5(1), 5-17 (2011-05-11)
    While precious metals are available to a very limited extent, there is an increasing demand to use them as catalyst. This is also true for palladium (Pd) catalysts and their sustainable recycling and production are required. Since Pd catalysts exist
    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
    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
    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
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