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(2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer manufacturers
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| | (2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer Basic information | | Reaction Application |
| Product Name: | (2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer | | Synonyms: | (2'-METHYLAMINO-1,1'-BIPHENYL-2-YL)METHANESULFONATOPALLADIUM(II)DIMER,MIN.98%;(2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer, min. 98%;(2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer;(2''-Methylamino-1,1''-biphenyl-2-yl)methanesulfonatopalladium(II) dimer;(2'-Methylamino-biphenyl-2-yl)methanesulfonatopalladium(II) dimer | | CAS: | 1581285-85-9 | | MF: | C28H30N2O6Pd2S2 | | MW: | 767.5176 | | EINECS: | | | Product Categories: | | | Mol File: | 1581285-85-9.mol |  |
| | (2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer Chemical Properties |
| form | Powder | | color | light gray | | Sensitive | air sensitive |
| | (2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer Usage And Synthesis |
| Reaction | Dimeric palladium precursor, that when treated with phosphines at room temperature in dichloromethane, provides Nsubstituted precatalysts. These catalysts are useful in the aminocarbonylation of (hetero)aryl bromides, and general C-C and C-N cross-coupling reactions.
| | Application | (2'-methylamino-1,1'-biphenyl-2-yl)methanesulfonylpalladium(II) dimer can be used as a palladium catalyst, mainly as a catalyst aid in organic synthesis. |
| | (2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer Preparation Products And Raw materials |
| Preparation Products | BrettPhos Pd G4-->XPhos Pd G4-->1-Butanone, 1-(4-fluorophenyl)-4-[(6bS,10aR)-2,3,6b,9,10,10a-hexahydro-3-methyl-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxalin-8(7H)-yl]--->t-BuXphos Palladacycle Gen. 4 |
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