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重要文件

662232

Sigma-Aldrich

N-杂环卡宾配体试剂盒 I

同義詞:

Heterocyclic Carbene Ligands

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About This Item

分類程式碼代碼:
12350000
NACRES:
NA.22
暫時無法取得訂價和供貨情況

反應適用性

core: palladium
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

套裝中的組件也可單獨購買

產品號碼
描述
SDS

  • 6566231,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride, 97% 1 gSDS

  • 6566311,3-Bis(2,4,6-trimethylphenyl)imidazolinium chloride, 95% 1 gSDS

  • 6600191,3-Diisopropylimidazolium tetrafluoroborate, 96% 1 gSDS

  • 6600351,3-Bis(1-adamantyl)imidazolium tetrafluoroborate, 97% 1 gSDS

象形圖

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訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析證明 (COA)

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文章

随着金属络合物催化的未活化底物的交叉偶联反应领域的快速进展,通过引入大量的非手性和手性膦配体化合物库,已变革了化学市场。

In collaboration with Umicore AG and Co.,1 we are pleased to offer a series of robust Pd(II) and Pd(0) complexes employed as the linchpin in C–C bond forming reactions.

Metal complex-catalyzed cross-coupling reactions of unactivated substrates introduce diverse phosphine ligands in chemical marketplace.

A wide range of NHC ligands are commonly available which exhibit high activities.

相關內容

In collaboration with Umicore AG and Co.,1 we are pleased to offer a series of robust Pd(II) and Pd(0) complexes employed as the linchpin in C–C bond forming reactions.

Questions

  1. What specific compounds are included in the N-Heterocyclic Carbene Ligands Kit I (662232)?

    1 answer
    1. The kit components can be found below the 'DESCRIPTION' section under 'Kit Components Also Available Separately'. This kit contains the following:

      1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride, 97% 1 g
      1,3-Bis(2,4,6-trimethylphenyl)imidazolinium chloride, 95% 1 g
      1,3-Diisopropylimidazolium tetrafluoroborate, 96% 1 g
      1,3-Bis(1-adamantyl)imidazolium tetrafluoroborate, 97% 1 g

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