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[IrCl (COE) 2]2

CAT: 0804-HY-W020887-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-W020887-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
[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.
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
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, protect from light, stored under nitrogen)
Scientific Category
Reference compound1
Clinical Information
No Development Reported

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