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Safety Information

GF43081174

Palladium

foil, not light tested, 100x100mm, thickness 0.0125mm, 99.95%

Synonym(s):

Palladium, PD000250

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1 EA
CN¥14,237.15

CN¥14,237.15

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1 EA
CN¥14,237.15

About This Item

Linear Formula:
Pd
CAS Number:
7440-05-3
Molecular Weight:
106.42
MDL number:
MFCD00011167
UNSPSC Code:
12141733
PubChem Substance ID:
329806578
NACRES:
NA.23

CN¥14,237.15

Please contact Customer Service for Availability
Request a Bulk Order

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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1 of 4

This Item
GF52079171GF51599425GF10106457
Palladium foil, not light tested, 100x100mm, thickness 0.0125mm, 99.95%

GF43081174

Palladium

Palladium foil, not light tested, 100x100mm, thickness 0.006mm, 99.95%

GF52079171

Palladium

Palladium foil, not light tested, 100x100mm, thickness 0.004mm, 99.95%

GF51599425

Palladium

Palladium foil, not light tested, 100x100mm, thickness 0.008mm, 99.95%

GF10106457

Palladium

form

foil

form

foil

form

foil

form

foil

manufacturer/tradename

Goodfellow 430-811-74

manufacturer/tradename

Goodfellow 520-791-71

manufacturer/tradename

Goodfellow 515-994-25

manufacturer/tradename

Goodfellow 101-064-57

bp

2970 °C (lit.)

bp

2970 °C (lit.)

bp

2970 °C (lit.)

bp

2970 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (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

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 Information

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    Xiao-Feng Wu et al.
    ChemSusChem, 6(2), 229-241 (2013-01-12)
    Palladium-catalyzed coupling reactions have become a powerful tool for advanced organic synthesis. This type of reaction is of significant value for the preparation of pharmaceuticals, agrochemicals, as well as advanced materials. Both, academic as well as industrial laboratories continuously investigate
    Palladium(II)-catalyzed alkene functionalization via nucleopalladation: stereochemical pathways and enantioselective catalytic applications.
    Richard I McDonald et al.
    Chemical reviews, 111(4), 2981-3019 (2011-03-25)
    Qing-An Chen et al.
    Chemical Society reviews, 42(2), 497-511 (2012-11-10)
    The transition metal catalyzed asymmetric hydrogenation of unsaturated compounds arguably presents one of the most attractive methods for the synthesis of chiral compounds. Over the last few decades, Pd has gradually grown up as a new and popular metal catalyst
    Pazhamalai Anbarasan et al.
    Chemical Society reviews, 40(10), 5049-5067 (2011-04-30)
    The palladium-catalyzed cyanation of Ar-X (X = I, Br, Cl, OTf, and H) allows for an efficient access towards benzonitriles. After its discovery in 1973 and following significant improvements in recent decades, this methodology has become nowadays the most popular
    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
    View All Related Papers

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