GF87742659
Rhodium
foil, not light tested, 25x25mm, thickness 0.001mm, permanent polyester support, 99.85%
Sinônimo(s):
Rhodium, RH000190
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About This Item
Fórmula empírica (Notação de Hill):
Rh
Número CAS:
Peso molecular:
102.91
Número MDL:
Código UNSPSC:
12141738
ID de substância PubChem:
NACRES:
NA.23
Ensaio
≥99.85%
forma
foil
fabricante/nome comercial
Goodfellow 877-426-59
resistividade
4.33 μΩ-cm, 20°C
pb
3727 °C (lit.)
pf
1966 °C (lit.)
densidade
12.41 g/cm3 (lit.)
cadeia de caracteres SMILES
[Rh]
InChI
1S/Rh
chave InChI
MHOVAHRLVXNVSD-UHFFFAOYSA-N
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Descrição geral
For updated SDS information please visit www.goodfellow.com.
Informações legais
Product of Goodfellow
Classe de risco de água (WGK)
nwg
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Certificados de análise (COA)
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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)
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
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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