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Home  > Bis(2-(3,5-dimethylphenyl)quinoline-C2,N')(acetylacetonato)iridium(III)

AE22274

1056874-46-4 | Bis(2-(3,5-dimethylphenyl)quinoline-C2,N')(acetylacetonato)iridium(III)

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $60.00 $42.00 -   +
250mg 95% in stock $137.00 $96.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE22274
Chemical Name: Bis(2-(3,5-dimethylphenyl)quinoline-C2,N')(acetylacetonato)iridium(III)
CAS Number: 1056874-46-4
Molecular Formula: C39H53IrN2O2
Molecular Weight: 774.0673
MDL Number: MFCD28144734
SMILES: CC1=CC(=[C-]2C(=C1)c1ccc3c(n1[Ir+3]142([O]=C(C)[CH-]C(=[O]1)C)[C-]1=C(C)C=C(C=C1c1n4c2ccccc2cc1)C)cccc3)C

 

Upstream Synthesis Route
  • Bis(2-(3,5-dimethylphenyl)quinoline-C2,N)(acetylacetonato)iridium(III) is a versatile and highly efficient catalyst commonly used in organic chemical synthesis. This complex plays a crucial role in promoting a variety of catalytic reactions, particularly in the realm of organic transformations.One key application of this catalyst lies in its ability to facilitate C-H activation reactions. By utilizing its iridium center, the complex can activate relatively inert C-H bonds in organic molecules, allowing for the selective functionalization of these bonds. This enables chemists to modify complex molecules in a controlled manner, leading to the synthesis of valuable intermediates and fine chemicals.Additionally, Bis(2-(3,5-dimethylphenyl)quinoline-C2,N)(acetylacetonato)iridium(III) exhibits remarkable activity in a range of cross-coupling reactions such as Suzuki-Miyaura, Heck, and Sonogashira couplings. These transformations are vital in the construction of carbon-carbon and carbon-heteroatom bonds, facilitating the creation of complex molecular architectures with high efficiency and selectivity.Furthermore, this catalyst has demonstrated exceptional performance in asymmetric catalysis, enabling the enantioselective synthesis of chiral compounds. Its ability to induce asymmetry in various transformations opens up new avenues for accessing biologically active molecules and pharmaceutical intermediates with high enantiomeric purity.Overall, Bis(2-(3,5-dimethylphenyl)quinoline-C2,N)(acetylacetonato)iridium(III) stands as a powerful tool in the hands of synthetic chemists, offering a wide range of applications in chemical synthesis and paving the way for the development of innovative and diverse compounds.
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