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CAS 671789-61-0

2,6-Bis(di-tert-butylphosphinoxy)phenylchlorohydroiridium(III) TCI B5033

2,6-Bis(di-tert-butylphosphinoxy)phenylchlorohydroiridium(III) TCI B5033

Chemical Identity

CAS No.
671789-61-0
PubChem
CID 132274833·SID 354333282
Formula
C22H40ClIrO2P2
Molecular weight
626.2 g/mol
Purity
>98.0%(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
ditert-butyl-(3-ditert-butylphosphanyloxybenzene-2-id-1-yl)oxyphosphane;hydride;iridium(3+);chloride
SMILES
[H-].CC(C)(C)P(C(C)(C)C)OC1=[C-]C(=CC=C1)OP(C(C)(C)C)C(C)(C)C.[Cl-].[Ir+3]
InChIKey
HELSKPCZFUCUCP-UHFFFAOYSA-M
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2,6-Bis(di-tert-butylphosphinoxy)phenylchlorohydroiridium(III) is a complex chemical compound widely used in catalysis and inorganic chemistry. It plays a crucial role in laboratory settings where C-H activation reactions are required. This compound is particularly valuable for its ability to facilitate chemical reactions without altering the fundamental structure of the substrate. Its application is essential in modern chemical research, especially in the synthesis of aromatic and heterocyclic compounds. Due to its unique properties, it is a preferred choice for researchers aiming to enhance reaction efficiency and selectivity.

The compound’s effectiveness stems from its molecular structure, which includes phosphinoxy groups attached to an iridium atom. This configuration provides high catalytic activity and stability, making it ideal for challenging chemical transformations. The specificity of its reactivity ensures minimal side reactions, thus improving the overall efficiency of chemical processes. Its chemical properties are highly targeted, allowing it to interact selectively with specific molecular sites. This makes it a reliable and efficient catalyst in various synthetic pathways.

In Indonesian laboratories, this compound is commonly used by chemists and researchers working in catalysis, organic synthesis, and inorganic chemistry. Its role is critical in advancing research that requires precise and efficient C-H activation. It is a key component in the development of new synthetic methods and the optimization of existing chemical processes. The compound’s reliability and performance make it a valuable asset in both academic and industrial research environments.

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  • C-H Activation Reactions: This compound is ideal for activating carbon-hydrogen bonds, enabling the synthesis of complex organic molecules with high selectivity.
  • Organic Synthesis: It is widely used in the creation of aromatic and heterocyclic compounds due to its ability to facilitate selective and efficient reactions.
  • Inorganic Chemistry Research: Its unique structure and catalytic properties make it a valuable tool for studying and manipulating inorganic chemical systems.
  • Catalytic Process Optimization: Researchers use it to enhance the efficiency of chemical reactions, reducing the need for excess reagents and improving yield.
  • Advanced Material Development: It plays a role in the development of new materials by enabling precise chemical modifications at the molecular level.

Brand TCI
CAS number 671789-61-0
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid powder or liquid, depending on the specific formulation
Storage —

This compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent moisture absorption and contamination. Due to its chemical reactivity, it should be handled with care using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to incompatible substances and ensure that storage conditions are consistent with standard laboratory safety protocols. Regular monitoring of storage conditions is advised to maintain the compound’s stability and effectiveness.

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