[IrCl (COE) 2]2

[IrCl (COE) 2]2 (Chlorobis (cyclooctene) iridium (I) dimer) is a transition metal catalyst with remarkable catalytic activity. It is widely used in catalyzing a variety of organic reactions, especially in the synthesis of unsaturated compounds. In addition, [IrCl (COE) 2]2 has shown potential anti-tumor properties in biochemical research.

Product Specifications

CAS Number

[12246-51-4]

Product Name Alternative

Chlorobis (cyclooctene) iridium (I) dimer

UNSPSC

12352300

Hazard Statement

H315, H319, H335

Target

Biochemical Assay Reagents; Endogenous Metabolite

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease; Others

Applications

Metabolism-protein/nucleotide metabolism

Assay Protocol

https://www.medchemexpress.com/ircl-coe-2-2.html

Purity

97.0

Smiles

[CH]1(CCCCCC2)=[CH]2[Ir+]134([CH]5=[CH]4CCCCCC5)[Cl-][Ir+]67([CH]8=[CH]6CCCCCC8)([CH]9=[CH]7CCCCCC9)[Cl-]3

Molecular Formula

C32H56Cl2Ir2

Molecular Weight

896.13

Precautions

H315, H319, H335

References & Citations

[1]Intermolecular, catalytic asymmetric hydroamination of bicyclic alkenes and dienes in high yield and enantioselectivity|[2]Transition-metal-catalyzed immobilization of organic functional groups onto solid supports through vinylsilane coupling reactions|[3]Iridium (I) -catalyzed hydrogen peroxide oxidation of hydroxamic acids and hetero DielsAlder reaction of the acyl nitroso intermediates with cyclopentadiene|[4]Alkylation of active methylene compounds with alcohols catalyzed by an iridium complex|[5]An efficient and recyclable catalytic system comprising nano-iridium (0) and a pyridinium salt of nido-carboranyldiphosphine for the synthesis of one-dimensional boronate esters via hydroboration reaction|[6]Allylic amination by a DNAdieneiridium (I) hybrid catalyst|[7]Versatile Pd (II) -Catalyzed C H Activation/Aryl Aryl Coupling of Benzoic and Phenyl Acetic Acids