Merck
Todas as fotos(2)

GF80841146

Rhodium

foil, 25x25mm, thickness 0.15mm, as rolled, 99.9%

Todas as fotos(2)
Sinônimo(s):
Rhodium, RH000235
Empirical Formula (Hill Notation):
Rh
Número CAS:
7440-16-6
Peso molecular:
102.91
Número MDL:
MFCD00011201
ID de substância PubChem:
329812114
NACRES:
NA.23

teor

99.9%

forma

foil

manufacturer/tradename

Goodfellow 808-411-46

resistividade

4.33 μΩ-cm, 20°C

tamanho × espessura

25 x 25 mm × 0.15 mm

pb

3727 °C (lit.)

pf

1966 °C (lit.)

densidade

12.41 g/cm3 (lit.)

SMILES string

[Rh]

InChI

1S/Rh

InChI key

MHOVAHRLVXNVSD-UHFFFAOYSA-N

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Descrição geral

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

Informações legais

Product of Goodfellow

Código de classe de armazenamento

13 - Non Combustible Solids

WGK

nwg

Ponto de fulgor (ºF)

Not applicable

Ponto de fulgor (ºC)

Not applicable

Certificado de análise

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Certificado de origem

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Mais documentos

Pressure-Temperature Nomograph
Structure Search

Quotes and Ordering

Bulk Quote-Order Product
Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation.
Denise A Colby et al.
Chemical reviews, 110(2), 624-655 (2009-05-15)
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
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
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
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
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