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GF01094374

Palladium

Name: Palladium
Brand: ALDRICH

foil, 8mm disks, thickness 0.0125mm, 99.95%

Sinónimos:

Palladium, PD000250

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About This Item

Fórmula lineal:

Número de CAS:

7440-05-3

Peso molecular:

106.42

MDL number:

MFCD00011167

UNSPSC Code:

12141733

PubChem Substance ID:

329800156

NACRES:

NA.23

assay

≥99.95%

form

foil

manufacturer/tradename

Goodfellow 010-943-74

resistivity

9.96 μΩ-cm, 20°C

L × thickness

8 mm × 0.0125 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

13 - Non Combustible Solids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

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Development of a second generation palladium-catalyzed cycloalkenylation and its application to bioactive natural product synthesis.

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

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)

Iodocyclization, followed by palladium-catalyzed coupling: a versatile strategy for heterocyclic library construction.

Anton V Dubrovskiy et al.

Combinatorial chemistry & high throughput screening, 15(6), 451-472 (2012-01-26)

The iodocyclization of functionally-substituted alkynes provides an excellent way to prepare a wide range of iodoheterocycles, which can then be readily elaborated through palladium-catalyzed Suzuki-Miyaura, Sonogashira, Heck, Hartwig-Buchwald, and carbonylation processes into libraries of medicinally relevant heterocycles. The synthesis of

High-valent organometallic copper and palladium in catalysis.

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

Synthesis of heterocycles via palladium-catalyzed carbonylations.

Xiao-Feng Wu et al.

Chemical reviews, 113(1), 1-35 (2012-10-09)

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