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GF36379345

Rhodium

foil, light tested, 15x15mm, thickness 0.05mm, as rolled, 99.9%

Sinônimo(s):

Rhodium, RH000210

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Sobre este item

Fórmula empírica (Notação de Hill):
Rh
Número CAS:
Peso molecular:
102.91
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12141738
MDL number:

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InChI

1S/Rh

SMILES string

[Rh]

InChI key

MHOVAHRLVXNVSD-UHFFFAOYSA-N

assay

99.9%

form

foil

manufacturer/tradename

Goodfellow 363-793-45

resistivity

4.33 μΩ-cm, 20°C

size × thickness

15x15 mm × 0.05 mm

bp

3727 °C (lit.)

mp

1966 °C (lit.)

density

12.41 g/cm3 (lit.)

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1 of 4

Este Item
GF57675561GF96356559GF24911726
Rhodium foil, light tested, 15x15mm, thickness 0.05mm, as rolled, 99.9%

GF36379345

Rhodium

Rhodium foil, light tested, 25x25mm, thickness 0.05mm, as rolled, 99.9%

GF57675561

Rhodium

Rhodium foil, light tested, 25x25mm, thickness 0.075mm, as rolled, 99.9%

GF96356559

Rhodium

Rhodium foil, not light tested, 25x25mm, thickness 0.012mm, as rolled, 99.9%

GF24911726

Rhodium

form

foil

form

foil

form

foil

form

foil

assay

99.9%

assay

99.9%

assay

≥99.9%

assay

99.90%

manufacturer/tradename

Goodfellow 363-793-45

manufacturer/tradename

Goodfellow 576-755-61

manufacturer/tradename

Goodfellow 963-565-59

manufacturer/tradename

Goodfellow 249-117-26

bp

3727 °C (lit.)

bp

3727 °C (lit.)

bp

3727 °C (lit.)

bp

3727 °C (lit.)

resistivity

4.33 μΩ-cm, 20°C

resistivity

4.33 μΩ-cm, 20°C

resistivity

4.33 μΩ-cm, 20°C

resistivity

4.33 μΩ-cm, 20°C

mp

1966 °C (lit.)

mp

1966 °C (lit.)

mp

1966 °C (lit.)

mp

1966 °C (lit.)

General description

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

Legal Information

Product of Goodfellow

Classe de armazenamento

13 - Non Combustible Solids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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Jerzy Klosin et al.
Accounts of chemical research, 40(12), 1251-1259 (2007-11-14)
A series of bis-phosphite and bis-phosphine ligands for asymmetric hydroformylation reactions has been evaluated. Bis-phosphite ligands lead, in general, to high regioselectivities across a range of substrates while good enantioselectivities are limited to only a few examples. We found that
Vladimir V Grushin
Accounts of chemical research, 43(1), 160-171 (2009-10-01)
Although springing from two established fields, organometallic chemistry and fluorine chemistry, organometallic fluorine chemistry is still in its early stages. However, developments in this area are expected to provide new tools for the synthesis of selectively fluorinated organic compounds that
Jeremy M Praetorius et al.
Dalton transactions (Cambridge, England : 2003), (31)(31), 4079-4094 (2008-08-09)
The organometallic chemistry of N-heterocyclic carbene complexes of the transition metals has received significant attention over the past ten years, especially with respect to complexes of Pd and Ru. The present Perspective highlights the chemistry of NHC complexes of another
Pablo Etayo et al.
Chemical Society reviews, 42(2), 728-754 (2012-11-08)
During the last few decades, rhodium-catalysed asymmetric hydrogenation of diverse alkene classes has emerged as a powerful synthetic tool in the pharmaceutical industry, contributing to the manufacturing of chiral drugs, recent drug candidates for clinical trials, and major synthetic precursors
Feng Shi et al.
Topics in current chemistry, 292, 123-164 (2010-01-01)
The catalytic activation of a C-H bond is a fundamentally important organic transformation. There are now numerous reports of palladium-mediated C-H activation by the through-space interaction of a palladium center with a neighboring C-H bond. This type of C-H activation

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