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Merck

GF82366342

foil, not light tested, 50x50mm, thickness 0.00025mm, permanent polyester support, 99.9%

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1 EA
$2,800.00

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预计发货时间2025年5月22日详情


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1 EA
$2,800.00

About This Item

经验公式(希尔记法):
Rh
CAS号:
分子量:
102.91
MDL编号:
UNSPSC代码:
12141738
PubChem化学物质编号:
NACRES:
NA.23

$2,800.00


预计发货时间2025年5月22日详情


获取大包装报价

方案

99.9%

表单

foil

制造商/商品名称

Goodfellow 823-663-42

电阻率

4.33 μΩ-cm, 20°C

尺寸 × 厚度

50 x 50 mm × 0.00025 mm

沸点

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

储存分类代码

13 - Non Combustible Solids

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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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