| Identification | Back Directory | [Name]
SPhos Pd G1, Methyl t-Butyl Ether Adduct | [CAS]
1028206-58-7 | [Synonyms]
SPhos precatalyst
SPhos Palladacycle
SPhos Pd G1, Methyl
SPhos Pd G1, Methyl t-Butyl Ether Adduct
Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II)
chloropalladium(1+),dicyclohexyl-[2-(2,6-dimethoxyphenyl)phenyl]phosphane,2-methoxy-2-methylpropane,2-phenylethanamine
Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct,S
Chloro(2-dicyclohexylphosphino-2',6'-diMethoxy-1,1'-biphenyl)[2-(2-aMinoethylphenyl)]palladiuM(II) - Methyl-t-butyl ether adduct
Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct, min. 98%
Palladium(II) acetate/2-dicyclohexylphosphino-26dimethoxy-1,1-biphenyl/potassium phosphate admixture [Catkit single-use vials - 1.96 wt% Pd(OAc)2]
Chloro(2-dicyclohexylphosphino-2',6'-diMethoxy-1,1'-biphenyl)[2-(2-aMinoethylphenyl)]palladiuM(II) Methyl-t-butylether adduct,98% SPhos Palladacycle
Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct, min. 98% [SPhos Palladacycle]
PalladiuM(II) acetate/2-dicyclohexylphosphino-2,6-diMethoxy-1,1'-biphenyl (SPhos)/potassiuM phosphate adMixture [CatKit single-use vials - 1.96 wt% Pd(OAc)2]
Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct, min. 98% [SPhos Palladacycle Gen. 1] | [Molecular Formula]
C34H45ClNO2PPd | [MDL Number]
MFCD15144765 | [MOL File]
1028206-58-7.mol | [Molecular Weight]
672.58 |
| Hazard Information | Back Directory | [Uses]
| [Uses]
Chloro(2-dicyclohexylphosphino-2'',6''-dimethoxy-1,1''-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) has been used as catalyst in, the studies of CDK 8/19 inhibitors: Discovery of novel and selective CDK8/19 dual inhibitors and elimination of their CYP3A4 time-dependent inhibition potential; ?Biaryl Phosphine Based Pd(II) Amido Complexes: The Effect of Ligand Structure on Reductive Elimination | [reaction suitability]
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
reaction type: Cross Couplings |
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