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GF14938005

Rhodium

microfoil, disks, 25mm, thinness 0.1μm, specific density 124μg/cm2, permanent mylar 3.5μm support, 99.9%

Sinonimo/i:

Rhodium, RH004500

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About This Item

Formula empirica (notazione di Hill):
Rh
Numero CAS:
7440-16-6
Peso molecolare:
102.91
Numero MDL:
MFCD00011201
Codice UNSPSC:
12141738
ID PubChem:
329802328
NACRES:
NA.23

Saggio

99.90%

Stato

foil

Produttore/marchio commerciale

Goodfellow 149-380-05

Resistività

4.33 μΩ-cm, 20°C

diam. × spessore

25 mm × 0.1 μm

P. ebollizione

3727 °C (lit.)

Punto di fusione

1966 °C (lit.)

Densità

12.41 g/cm3 (lit.)

Stringa SMILE

[Rh]

InChI

1S/Rh
MHOVAHRLVXNVSD-UHFFFAOYSA-N

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Descrizione generale

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

Note legali

Product of Goodfellow

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

nwg

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Huw M L Davies et al.
Chemical Society reviews, 36(7), 1109-1119 (2007-06-20)
This tutorial review describes the reactions of the electron-rich heterocycles pyrrole, furan, indole and benzofuran with copper and rhodium carbenoids. Two main reaction pathways are possible, involving either a concerted non-synchronous cyclopropanation or zwitterionic intermediates. A diverse range of products
Jan Meine Ernsting et al.
Magnetic resonance in chemistry : MRC, 42(9), 721-736 (2004-08-13)
Rhodium is used for a number of large processes that rely on homogeneous rhodium-catalyzed reactions, for instance rhodium-catalyzed hydroformylation of alkenes, carbonylation of methanol to acetic acid and hydrodesulfurization of thiophene derivatives (in crude oil). Many laboratory applications in organometallic
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
Huw M L Davies et al.
Chemical Society reviews, 40(4), 1857-1869 (2011-03-02)
This tutorial review presents a description of the controlling elements of intermolecular C-H functionalization by means of C-H insertion by donor/acceptor rhodium carbenes. These rhodium carbenes, readily derived from the combination of diazo compounds with dirhodium(ii) catalysts, are sufficiently reactive
Jean Bouffard et al.
Topics in current chemistry, 292, 231-280 (2010-01-01)
A review is presented of synthetic methods for the preparation of biaryls by the rhodium-catalyzed C-H bond arylation of arenes with aryl halides (C-H/ C-X couplings), arylmetal reagents (C-H/C-M couplings) and arenes (C-H/C-H couplings), with an emphasis on postulated mechanisms
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Global Trade Item Number

SKUGTIN
GF14938005-2EA4061829495213
GF14938005-10EA4061829475345
GF14938005-1EA4061825356983
GF14938005-5EA4061829556501

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