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Product Name:2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole, min. 98% CM-Phos CAS:1067883-58-2 Purity:min. 98% Package:100mg;500mg
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| 2-(2-Dicyclohexylphosphanyl-phenyl)-1-Methyl-1H-indole Basic information | Reaction |
| 2-(2-Dicyclohexylphosphanyl-phenyl)-1-Methyl-1H-indole Chemical Properties |
Melting point | 180-185℃ | Boiling point | 582.4±33.0 °C(Predicted) | form | Powder | color | white to off-white | CAS DataBase Reference | 1067883-58-2 |
| 2-(2-Dicyclohexylphosphanyl-phenyl)-1-Methyl-1H-indole Usage And Synthesis |
Reaction |
- Suzuki-Miyaura Coupling of Aryl Mesylates and alkenyl tosylate and mesylate bearing alkyl, methoxy, aldehyde, keto, nitrile, ester, and heteroaryl substitution.
- Sonogashira Coupling of Aryl Mesylates, R' = alkyl, aryl; R = C(O)R, COOMe, CHO, CN.
- Buchwald-Hartwig Amination of Aryl Mesylates, R = cyano, chloro, methoxy, keto, ester and etc.
- Additional catalyzed reactions include Cyanation of functional Aryl Mesylates and Chlorides; Hiyama Coupling of Aryl Mesylates; Direct Arylation of Heterocycles with Aryl Mesylates; Borylation of Aryl Mesylates.
| Uses | 2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole (CM-Phos) is an organic compound with catalytic activity. 2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole can be used as an efficient catalyst for cross-coupling reactions of various alcohols and olefins. 2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole shows important application potential in pharmaceutical and material science. | reaction suitability | 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: ligand |
| 2-(2-Dicyclohexylphosphanyl-phenyl)-1-Methyl-1H-indole Preparation Products And Raw materials |
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