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Merck

GF89451489

rod, 50mm, diameter 2.0mm, 99.95%

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1 EA
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1 EA
$1,430.00

About This Item

线性分子式:
Pd
CAS号:
分子量:
106.42
MDL编号:
UNSPSC代码:
12141733
PubChem化学物质编号:
NACRES:
NA.23

$1,430.00


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方案

≥99.95%

表单

rod

制造商/商品名称

Goodfellow 894-514-89

电阻率

9.96 μΩ-cm, 20°C

沸点

2970 °C (lit.)

mp

1554 °C (lit.)

密度

12.02 g/cm3 (lit.)

SMILES字符串

[Pd]

InChI

1S/Pd

InChI key

KDLHZDBZIXYQEI-UHFFFAOYSA-N

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一般描述

For updated SDS information please visit www.goodfellow.com.

法律信息

Product of Goodfellow

储存分类代码

13 - Non Combustible Solids

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
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
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
Keary M Engle et al.
The Journal of organic chemistry, 78(18), 8927-8955 (2013-04-10)
Homogeneous transition-metal-catalyzed reactions are indispensable to all facets of modern chemical synthesis. It is thus difficult to imagine that for much of the early 20th century, the reactivity and selectivity of all known homogeneous metal catalysts paled in comparison to

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