GF14938005
Rhodium
microfoil, disks, 25mm, thinness 0.1μm, specific density 124μg/cm2, permanent mylar 3.5μm support, 99.9%
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Sinônimo(s):
Rhodium, RH004500
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
99.90%
forma
foil
fabricante/nome comercial
Goodfellow 149-380-05
resistividade
4.33 μΩ-cm, 20°C
diâmetro × espessura
25 mm × 0.1 μm
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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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
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
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
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
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
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