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Merck
CN

900277

Sigma-Aldrich

双(3,5-双(三氟甲基)苯基)(2′,6′-双(二甲基氨基)-3,6-二甲氧基联苯-2-基)膦

≥95%

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别名:
2′-(双(3,5-双(三氟甲基)苯基)膦酰基)-3′,6′-二甲氧基-N ,N ,N ,N -四甲基l-[1,1′-联苯] -2,6-二胺, 2′-(双(3,5-双(三氟甲基)苯基)膦酰基)-3′,6′-二甲氧基N2,N2,N6,N6 -四甲基-[1,1′-联苯] -2,6-二胺, 2- {双[3,5-双(三氟甲基)苯基]膦基} -3,6-二甲氧基 -2′,6′-双(二甲基氨基)-1,1′- 联苯
经验公式(希尔记法):
C34H29F12N2O2P
分子量:
756.56
UNSPSC代码:
12352128
NACRES:
NA.22

质量水平

检测方案

≥95%

形式

powder or crystals

反应适用性

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
reaction type: Cross Couplings

reagent type: ligand

mp

160.3 °C

官能团

phosphine

应用

作为Pd G4络合物,来自Buchwald小组的这类催化剂在空间受阻的仲胺的芳基化反应中提供了同类产品中最佳的反应活性。

危险声明

危险分类

Aquatic Chronic 4

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Nathaniel H Park et al.
Angewandte Chemie (International ed. in English), 54(28), 8259-8262 (2015-06-03)
In Pd-catalyzed C-N cross-coupling reactions, α-branched secondary amines are difficult coupling partners and the desired products are often produced in low yields. In order to provide a robust method for accessing N-aryl α-branched tertiary amines, new catalysts have been designed

相关内容

The Buchwald group has developed a series of highly active and versatile palladium precatalysts and biarylphosphine ligands used in cross-coupling reactions for the formation of C-C, C–N, C–O, C–F, C–CF3, and C–S bonds. The ligands are electron-rich, and highly tunable to provide catalyst systems with a diverse scope, high stability and reactivity. Furthermore, the new series of precatalysts are air-, moisture and thermally-stable and display good solubility in common organic solvents. The use of precatalysts ensures the efficient generation of the active catalytic species and allows one to accurately adjust the ligand:palladium ratio. The ligands, precatalysts and methodology developed in the Buchwald group are user friendly and have rendered previously difficult cross couplings reactions, much easier to achieve.

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