推荐产品
表单
liquid
质量水平
反应适用性
core: manganese
reagent type: catalyst
浓度
0.5 M in THF
密度
0.956 g/mL at 25 °C
SMILES字符串
[Li+].[Li+].Cl[Mn--](Cl)(Cl)Cl
InChI
1S/4ClH.2Li.Mn/h4*1H;;;/q;;;;2*+1;+2/p-4
InChI key
VJOUQNFWQPCDPE-UHFFFAOYSA-J
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应用
Catalyst for homocoupling of Grignard reagents using atmospheric oxygen as an oxidant
Reactant for:
Reagent for the preparation of Rieke manganese
Reactant for:
- Transmetalation reactions
- Nickel-imidazolium carbene-catalyzed coupling reactions
Reagent for the preparation of Rieke manganese
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
补充剂危害
储存分类代码
3 - Flammable liquids
WGK
WGK 3
闪点(°F)
1.4 °F - closed cup
闪点(°C)
-17.0 °C - closed cup
法规信息
危险化学品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
José M Concellón et al.
The Journal of organic chemistry, 72(21), 7974-7979 (2007-09-25)
A complete E-selective synthesis of alpha,beta-unsaturated amides through a sequential reaction of a range of dichloroamides with a variety of aldehydes promoted by Rieke manganese (Mn*) is reported. A mechanism based on a sequential aldol-type reaction and a completely stereoselective
A. Eloi, et al.,
Organometallics, 28, 925-928 (2009)
Manganese- or iron-catalyzed homocoupling of grignard reagents using atmospheric oxygen as an oxidant.
Gérard Cahiez et al.
Journal of the American Chemical Society, 129(45), 13788-13789 (2007-10-20)
A. Leleu, et al.,
Advanced Synthesis & Catalysis, 348, 1086-1092 (2006)
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