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GF52079171

Palladium

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

Synonym(s):

Palladium, PD000200

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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:
329807869
NACRES:
NA.23

Assay

99.95%

form

foil

manufacturer/tradename

Goodfellow 520-791-71

resistivity

9.96 μΩ-cm, 20°C

size × thickness

100x100 mm × 0.006 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
Stephan Enthaler et al.
Chemical Society reviews, 40(10), 4912-4924 (2011-06-07)
The formation of oxygen-carbon bonds is one of the fundamental transformations in organic synthesis. In this regard the application of palladium-based catalysts has been extensively studied during recent years. Nowadays it is an established methodology and the success has been
Kiyofumi Inamoto
Chemical & pharmaceutical bulletin, 61(10), 987-996 (2013-10-04)
Herein, we describe our development of synthetic methods for heterocyclic compounds based on the palladium-catalyzed carbon-hydrogen bond (C-H) functionalization/intramolecular carbon-heteroatom (nitrogen or sulfur) bond formation process. By this C-H cyclization method, we efficiently prepared various N-heterocycles, including indazoles, indoles, and
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