Identification | Back Directory | [Name]
2′-(Amino-κN)[1,1′-biphenyl]-2-yl-κC][2′-[(1,1-dimethylethyl)phenylphosphino-κP]-N2,N2,N6,N6-tetramethyl[1,1′-biphenyl]-2,6-diamine](methanesulfonato-κO)palladium | [CAS]
1661042-31-4 | [Synonyms]
2′-(Amino-κN)[1,1′-biphenyl]-2-yl-κC][2′-[(1,1-dimethylethyl)phenylphosphino-κP]-N2,N2,N6,N6-tetramethyl[1,1′-biphenyl]-2,6-diamine](methanesulfonato-κO)palladium 2'-(Amino-κN)[1,1'-biphenyl]-2-yl-κC][2'-[(1,1-dimethylethyl)phenylphosphino-κP]-N2,N2,N6,N6-tetramethyl[1,1'-biphenyl]-2,6-diamine](methanesulfonato-κO)palladium Palladium, [2′-(amino-κN)[1,1′-biphenyl]-2-yl-κC][2′-[(1,1-dimethylethyl)phenylphosphino-κP]-N2,N2,N6,N6-tetramethyl[1,1′-biphenyl]-2,6-diamine](methanesulfonato-κO)- | [Molecular Formula]
C39H46N3O3PPdS | [MDL Number]
MFCD31560638 | [MOL File]
1661042-31-4.mol | [Molecular Weight]
774.27 |
Hazard Information | Back Directory | [Uses]
As the Pd G3 complex, this ligand from the Buchwald group offers best-in-class performance in the arylation of sterically hindered primary amines. | [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: catalyst reaction type: Cross Couplings |
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