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Merck
모든 사진(2)

Key Documents

GF43148280

Palladium

foil, 0.2m coil, thickness 0.1mm, coil width 2mm, as rolled, 99.95%

동의어(들):

Palladium, PD000276

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About This Item

Linear Formula:
Pd
CAS Number:
Molecular Weight:
106.42
MDL number:
UNSPSC 코드:
12141733
PubChem Substance ID:
NACRES:
NA.23

분석

99.95%

형태

foil

제조업체/상표

Goodfellow 431-482-80

저항도

9.96 μΩ-cm, 20°C

길이 × 두께 × 너비

0.2 m × 0.1 m × 2 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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For updated SDS information please visit www.goodfellow.com.

법적 정보

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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문서 라이브러리 방문

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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