| Identification | Back Directory | [Name]
Chloro[(tricyclohexylphosphine)-2-(2'-aminobiphenyl)]palladium(II) | [CAS]
1353658-81-7 | [Synonyms]
PCy3 Pd G2
PCy3 Palladacycle Gen.2
Tricyclohexylphosphine Pd G2
Chloro[(tricyclohexylphosphine)-2-(2'-aminobiphenyl)]palladium(II)
Chloro[(tricyclohexylphosphine)(2'-aminobiphenyl-2-yl)palladium(II)
Chloro[(tricyclohexylphosphine)(2'-aminobiphenyl-2-yl)palladium(II) / PCy3 Pd G2
(SP-4-3)-[2'-(Amino)[1,1'-biphenyl]-2-yl]chloro(tricyclohexylphosphine)palladium
(SP-4-3)-[2'-(Amino-κN)[1,1'-biphenyl]-2-yl-κC]chloro(tricyclohexylphosphine)palladium
Chloro[(tricyclohexylphosphine)-2-(2'-aminobiphenyl)]palladium(II) ISO 9001：2015 REACH | [Molecular Formula]
C30H42ClNPPd+2 | [MDL Number]
MFCD21363051 | [MOL File]
1353658-81-7.mol | [Molecular Weight]
589.508 |
| Hazard Information | Back Directory | [Uses]
PCy3 Pd G2 is a monophosphine-coordinated 2-phenylaniline-based palladacycle complex that can be used as a precatalyst:
- To prepare diarylmethanes by Suzuki cross-coupling reaction with heterocyclic-chloromethyl derivatives with aryl/heteroaryl boronic acids.
- To synthesize poly(arylene)s by the Suzuki cross-coupling polymerization reaction between aryl dihalides and aryldiboronic acids.
- In the C-H bond functionalization reactions.
| [reaction suitability]
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: C-H Activation
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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