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CAS 14592-56-4

Bis(acetonitrile)palladium(II) Dichloride TCI B1676

Bis(acetonitrile)palladium(II) Dichloride TCI B1676

Chemical Identity

CAS No.
14592-56-4
PubChem
CID 84541·SID 87564577
Formula
C4H6Cl2N2Pd
Molecular weight
259.43 g/mol
Purity
>98.0%(T)
Reference databases
ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
bis(acetonitrile);palladium(2+);dichloride
SMILES
CC#N.CC#N.[Cl-].[Cl-].[Pd+2]
InChIKey
RBYGDVHOECIAFC-UHFFFAOYSA-L
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Bis(acetonitrile)palladium(II) Dichloride is a chemical compound widely used in catalytic reactions, particularly in C-H activation processes. This material functions as a metal-based catalyst, playing a crucial role in various organic and inorganic chemical reactions that require the activation of carbon-hydrogen bonds. Its unique structure allows for strong interactions with reaction substrates, making it highly effective in promoting complex chemical transformations. In laboratory settings, it is a key reagent for advancing research in catalytic chemistry and synthetic methodologies.

The compound's reactivity and specificity make it a preferred choice for researchers working on advanced catalytic systems. Its ability to facilitate cross-coupling reactions, oxidation processes, and substitution reactions highlights its versatility in chemical synthesis. Additionally, its structural complexity enables it to act as a versatile catalyst in a wide range of applications. These properties make it an essential tool for scientists aiming to develop new chemical processes and materials.

In Indonesian laboratories, Bis(acetonitrile)palladium(II) Dichloride is commonly used in organic and inorganic chemistry research, especially in C-H activation and the synthesis of complex compounds. Its availability in small pack sizes, such as 1 gram, ensures ease of use in laboratory-scale experiments. Researchers in Indonesia rely on this compound for its efficiency and reliability in catalytic applications.

  • C-H Activation Reactions: This compound is ideal for activating carbon-hydrogen bonds, enabling the formation of new chemical bonds in complex molecules.
  • Cross-Coupling Reactions: Its catalytic properties make it suitable for facilitating cross-coupling reactions, which are essential in organic synthesis.
  • Oxidation Processes: It is effective in promoting oxidation reactions, allowing for the transformation of various organic compounds.
  • Substitution Reactions: Its reactivity enables it to act as a catalyst in substitution reactions, enhancing the efficiency of synthetic pathways.
  • Complex Compound Synthesis: The compound is frequently used in the synthesis of complex organic and inorganic compounds due to its catalytic versatility.

From the TCI brochure

  • Palladium catalyst in alkyl sulfone synthesis scheme with P2480

Brand TCI
CAS number 14592-56-4
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack sizes 1 gram
Physical form Solid
Storage —

This compound should be stored in a dry, cool environment away from moisture and oxidizing agents to maintain its stability. It is recommended to use airtight containers to prevent exposure to humidity, which can degrade its effectiveness. Due to its reactivity, it should be handled with care using appropriate personal protective equipment. Storage in a controlled laboratory environment ensures optimal performance and safety. Regular monitoring of storage conditions is advised to maintain the compound's integrity and usability in experimental applications.

References cited in the TCI brochure

  1. Rammohan Devulapally. Synthesis and cross-coupling reactions of imidomethyltrifluoroborates with aryl chlorides Tetrahedron Letters, 2012. doi:10.1016/j.tetlet.2011.12.062