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Safety Information

GF47424528

Palladium

microfoil, disks, 25mm, thinness 0.1μm, specific density 119.2μg/cm2, permanent mylar 3.5μm support, 99.99%

Synonym(s):

Palladium, PD004500

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5 G
CN¥419.64
10 G
CN¥656.72
50 G
CN¥1,803.15

CN¥419.64

Estimated to ship onMay 23, 2025Details

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5 G
CN¥419.64
10 G
CN¥656.72
50 G
CN¥1,803.15

About This Item

Linear Formula:
Pd
CAS Number:
7440-05-3
Molecular Weight:
106.42
MDL number:
MFCD00011167
UNSPSC Code:
12141733
PubChem Substance ID:
329807163
NACRES:
NA.23

CN¥419.64

Estimated to ship onMay 23, 2025Details

Request a Bulk Order

Assay

99.99%

form

foil

manufacturer/tradename

Goodfellow 474-245-28

resistivity

9.96 μΩ-cm, 20°C

diam. × thickness

25 mm × 0.1 μm

bp

2970 °C (lit.)

mp

1554 °C (lit.)

density

12.02 g/cm3 (lit.)

SMILES string

[Pd]

InChI

1S/Pd

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Show Differences

1 of 4

This Item
D163708274992N9125
N-甲基羟胺 盐酸盐 98%

M50400

N-甲基羟胺 盐酸盐

N,O-二甲基羟胺 盐酸盐 98%

D163708

N,O-二甲基羟胺 盐酸盐

O-乙基羟胺 盐酸盐 97%

274992

O-乙基羟胺 盐酸盐

N-(1-萘基)乙二胺 二盐酸盐 ≥98%

N9125

N-(1-萘基)乙二胺 二盐酸盐

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

mp

86-88 °C (lit.)

mp

112-115 °C

mp

130-133 °C (lit.)

mp

194-198 °C (dec.) (lit.)

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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    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)
    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
    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
    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
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