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900699 Sigma-Aldrich

(tBu)2PPh Pd G4

≥95%

  • Empirical Formula (Hill Notation) C28H38NO3PPdS

  • Molecular Weight 606.07

  •  NACRES NA.22

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Properties

Related Categories Buchwald 4th Generation Palladacycles, Buchwald Ligands and Complexes, Catalysis and Inorganic Chemistry, Chemical Synthesis, Cross-Coupling More...
Quality Level   100
assay   ≥95%
form   powder
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
mp   152-158 °C
functional group   phosphine

Description

Application

(tBu)2PPh Pd G4 is a powerful ligand for classic cross-coupling reactions combined with the Buchwald Fourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

Packaging

1 g in glass insert

250 mg in glass insert

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

Organic Optoelectronics on Shape Memory Polymers

Center for Organic Photonics and Electronics (COPE), School of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, USA *E-mail: bernard.kippelen@ece.gatech.e...
Canek Fuentes-Hernandez, Bernard Kippelen*
Material Matters, 2017, 12.3
Keywords: AGE, Adhesion, Atomic layer deposition, Biological processes, Catalysis, Ceramics, Deposition, Electronics, Environmental, Nanomaterials, Nanotubes, Oxidations, Photovoltaics, Polymerization reactions, Reductions, Semiconductor, Separation

Stephen Buchwald Group – Professor Product Portal

From our library of Articles, Sigma-Aldrich presents Stephen Buchwald Group – Professor Product Portal
Keywords: Aminations, Asymmetric catalysis, Asymmetric synthesis, Catalysis, Coupling reactions, Cross couplings, Fluorinations, Ligands, Solvents, transformation

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