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Merck
CN

GF57675561

foil, light tested, 25x25mm, thickness 0.05mm, as rolled, 99.9%

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别名:
经验公式(希尔记法):
Rh
CAS号:
分子量:
102.91
MDL编号:
UNSPSC代码:
12352300
PubChem化学物质编号:
NACRES:
NA.23

检测方案

99.9%

形式

foil

制造商/商品名称

Goodfellow 576-755-61

电阻率

4.33 μΩ-cm, 20°C

尺寸 × 厚度

25x25 mm × 0.05 mm

bp

3727 °C (lit.)

mp

1966 °C (lit.)

密度

12.41 g/cm3 (lit.)

SMILES字符串

[Rh]

InChI

1S/Rh

InChI key

MHOVAHRLVXNVSD-UHFFFAOYSA-N

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一般描述

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

法律信息

Product of Goodfellow

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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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
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)

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