| Identification | Back Directory | [Name]
2'-(DIMETHYLAMINO)-2-BIPHENYLYL-PALLADIUM(II) CHLORIDE DINORBORNYLPHOSPHINE COMPLEX | [CAS]
359803-53-5 | [Synonyms]
SK-CC01-A
2'-(DIMETHYLAMINO)-2-BIPHENYLYL-PD(II)-CL DINORBORNYLPHOSPH.
CHLORO-[2'-(DIMETHYLAMINO)-2-BIPHENYLYL]-(DINORBORNYLPHOSPHINE)-PALLADIUM
CHLORO(DI-2-NORBORNYLPHOSPHINO)(2'-DIMETHYLAMINO-1,1'-BIPHENYL-2-YL)PALLADIUM
CHLORO(DI-2-NORBORNYLPHOSPHINO)(2'-DIMETHYLAMINO-1,1'-BIPHENYL-2-YL)PALLADIUM(II)
2'-(Dimethylamino)-2-biphenyl-palladium(II)-chloride dinorbornylphosphine complex
2'-(Dimethylamino)-2-biphenylyl-palladium(Ⅱ) chloride dinorbornylphosphine complex
2'-(DIMETHYLAMINO)-2-BIPHENYLYL-PALLADIUM(II) CHLORIDE DINORBORNYLPHOSPHINE COMPLEX
SK-CC01-A, Chloro-[2μ-(dimethylamino)-2-biphenylyl]-(dinorbornylphosphine)-palladium
Chloro(di-2-norbornylphosphino)(2'-diMethylaMino-1,1'-biphenyl-2-yl)palladiuM(II),97%
Chloro(di-2-norbornylphosphino)(2'-diMethylaMino-1,1'-biphenyl-2-yl)palladiuM(II) Min.
Chloro(di-2-norbornylphosphino)(2'-dimethylamino-1,1'-biphenyl-2-yl)palladium(II),97%min.
2'-(Dimethylamino)-2-biphenylyl-palladium(II) chloride Dinorbornylphosphine complex >=99.0% (C) | [Molecular Formula]
C28H37ClNPPd | [MDL Number]
MFCD03427335 | [MOL File]
359803-53-5.mol | [Molecular Weight]
560.45 |
| Chemical Properties | Back Directory | [Melting point ]
160-170 °C (dec.)(lit.)
| [form ]
Powder | [color ]
beige | [InChIKey]
YMZCYRNVJBOOCT-SBADXZPPSA-M | [SMILES]
C1C[C@@H]2C[C@H]1CC2PC3C[C@@H]4CC[C@H]3C4.CN(C)c5ccccc5-c6ccccc6[Pd]Cl |
| Hazard Information | Back Directory | [Chemical Properties]
Light grey powder | [reaction suitability]
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
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 |
| Questions And Answer | Back Directory | [Reactions]
A new, air and moisture-stable, palladium catalyst useful in a broad scope of C-C and C-N coupling reactions. The highlyactive catalyst can tolerate substrates containing a wide variety of functional groups such as alkyls, alkoxides, ketones, aldehydes, esters, amines, trifluoromethyl and nitro groups.
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