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Merck
CN

302473

Sigma-Aldrich

双环辛烯氯化铑二聚体

98%, powder

别名:

[Rh(coe)2Cl]2

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关于此项目

经验公式(希尔记法):
C32H56Cl2Rh2
化学文摘社编号:
分子量:
717.50
MDL编号:
UNSPSC代码:
12161600
PubChem化学物质编号:
NACRES:
NA.22
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产品名称

双环辛烯氯化铑二聚体, 98%

质量水平

方案

98%

表单

powder

反应适用性

core: rhodium
reagent type: catalyst

mp

190 °C (dec.) (lit.)

SMILES字符串

Cl[Rh].Cl[Rh].C1CCCC=CCC1.C2CCCC=CCC2.C3CCCC=CCC3.C4CCCC=CCC4

InChI

1S/4C8H14.2ClH.2Rh/c4*1-2-4-6-8-7-5-3-1;;;;/h4*1-2H,3-8H2;2*1H;;/q;;;;;;2*+1/p-2/b4*2-1-;;;;

InChI key

GQPAPAIPOLEZHT-XFCUKONHSA-L

应用

双环辛烯氯化铑(I)二聚体可用作以下反应的催化剂:
  • 通过芳基硼酸与α,β-不饱和磺酰基化合物的不对称1,4-加成,合成富对映体的偕二芳基磺酸盐。
  • N脱保护吲哚和吡咯的直接C-芳基化。
  • 通过C-H键活化的在芳烃羧化反应。

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Direct C-arylation of free (NH)-indoles and pyrroles catalyzed by Ar- Rh (III) complexes assembled in situ
Wang X, et al.
Journal of the American Chemical Society, 127(14), 4996-4997 (2005)
Chiral Phosphite-Olefin Ligands: Application in Rh-Catalyzed Asymmetric 1, 4-Addition of Arylboronic Acids to beta-Aryl-alpha, beta-unsaturated Sulfonates
Yue-Na Y and Ming-Hua X
Acta Chimica Sinica , 72(7), 815-819 (2014)
Rhodium (I)-catalyzed direct carboxylation of arenes with CO2 via chelation-assisted C- H bond activation
Mizuno H, et al.
Journal of the American Chemical Society, 133(5), 1251-1253 (2011)
Jay A Labinger et al.
Nature, 417(6888), 507-514 (2002-05-31)
The selective transformation of ubiquitous but inert C H bonds to other functional groups has far-reaching practical implications, ranging from more efficient strategies for fine chemical synthesis to the replacement of current petrochemical feedstocks by less expensive and more readily
Fumitoshi Kakiuchi et al.
Accounts of chemical research, 35(10), 826-834 (2002-10-16)
The cleavage and addition of ortho C-H bonds in various aromatic compounds such as ketones, esters, imines, imidates, nitrile, and aldehydes to olefins and acetlylenes can be achieved catalytically with the aid of ruthenium catalysts. The reaction is generally highly

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Discover the role of boronic acids in enantioenriched C(sp2)–C(sp2) product synthesis, specifically the rhodium-catalyzed Suzuki–Miyaura-type arylations of allylic halides and cyclobutenes.

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