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CAS 59831-02-6

[1,3-Bis(diphenylphosphino)propane]palladium(II) Dichloride TCI B2192

[1,3-Bis(diphenylphosphino)propane]palladium(II) Dichloride TCI B2192

Chemical Identity

CAS No.
59831-02-6
PubChem
CID 9916497·SID 87565052
Formula
C27H26Cl2P2Pd
Molecular weight
589.8 g/mol
Purity
>98.0%(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3-diphenylphosphanylpropyl(diphenyl)phosphane;palladium(2+);dichloride
SMILES
C1=CC=C(C=C1)P(CCCP(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4.[Cl-].[Cl-].[Pd+2]
InChIKey
LDFBXJODFADZBN-UHFFFAOYSA-L
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TCI B2192 59831-02-6 [1,3-Bis(diphenylphosphino)propane]palladium(II) Dichloride is a chemical compound widely used in catalytic reactions, particularly in C-H activation. This material plays a crucial role in modern laboratory settings by facilitating complex organic transformations with high efficiency. It is a metal complex that enables the selective activation of carbon-hydrogen bonds, which is essential in the synthesis of various organic compounds. Its application spans multiple areas of chemical research, making it a versatile reagent for advanced synthetic processes.

The compound's unique properties make it a preferred choice in laboratory environments. Its molecular structure allows for strong interactions with substrates, enhancing reaction efficiency. The compound exhibits excellent stability under various reaction conditions, ensuring consistent performance. Additionally, its high catalytic activity reduces the need for excessive reagent usage, making it both effective and cost-efficient. These characteristics contribute to its widespread use in both academic and industrial research settings.

In Indonesian laboratories, this compound is highly relevant for organic chemistry and catalysis research. It is commonly used in experiments requiring efficient catalytic reactions, especially in the development of new synthetic methodologies. Due to its reliability and effectiveness, it is a preferred material for researchers working on advanced chemical processes and C-H activation studies.

TCI brochures (PDF)

  • C-H Activation Reactions: This compound is ideal for activating carbon-hydrogen bonds, enabling selective and efficient transformations in complex organic molecules.
  • Organic Synthesis: Its catalytic properties make it suitable for synthesizing a wide range of organic compounds, including pharmaceuticals and fine chemicals.
  • Catalytic Cross-Coupling Reactions: The compound is used in cross-coupling reactions to form carbon-carbon bonds, which is critical in the synthesis of complex molecules.
  • Green Chemistry Initiatives: Its high efficiency reduces waste and reagent usage, aligning with sustainable and environmentally friendly laboratory practices.
  • Academic Research: It is widely used in university and research institutions for teaching and experimental studies in catalytic chemistry.

Brand TCI
CAS number 59831-02-6
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack sizes Available in various quantities as per standard laboratory requirements
Physical form Solid powder
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can degrade its properties. Suitable storage containers include glass or high-density polyethylene (HDPE) bottles with airtight closures. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid contact with incompatible materials and ensure proper ventilation in the workspace. Regular monitoring of storage conditions is advised to maintain the compound’s integrity and performance in laboratory applications.

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