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Merck

GF87742659

Rhodium

foil, not light tested, 25x25mm, thickness 0.001mm, permanent polyester support, 99.85%

Synonym(e):

Rhodium

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About This Item

Empirische Formel (Hill-System):
Rh
CAS-Nummer:
Molekulargewicht:
102.91
MDL-Nummer:
UNSPSC-Code:
12141738
PubChem Substanz-ID:
NACRES:
NA.23

Assay

≥99.85%

Form

foil

Hersteller/Markenname

Goodfellow 877-426-59

Widerstandsfähigkeit

4.33 μΩ-cm, 20°C

bp

3727 °C (lit.)

mp (Schmelzpunkt)

1966 °C (lit.)

Dichte

12.41 g/cm3 (lit.)

SMILES String

[Rh]

InChI

1S/Rh

InChIKey

MHOVAHRLVXNVSD-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Rechtliche Hinweise

Product of Goodfellow

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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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
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
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
Albert Padwa
Chemical Society reviews, 38(11), 3072-3081 (2009-10-23)
In this tutorial review, the rhodium(II)-catalyzed domino reactions of alpha-diazo carbonyl compounds are summarized. The article will emphasize some of the more recent synthetic applications of the rhodium carbenoid cyclization/cycloaddition domino cascade for alkaloid synthesis. The many structurally diverse and
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

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