(Pentamethylcyclopentadienyl)iridium(III) chloride dimer

(Pentamethylcyclopentadienyl)iridium(III) chloride dimer Basic information
Reaction
Product Name:(Pentamethylcyclopentadienyl)iridium(III) chloride dimer
Synonyms:(PentaMethylcyclopentadienyl)iridiuM(III) chloride diMer, 99% 250MG;PentaMethylcyclopentadienyl)iridiuM(III) chloride diMer,98% (Cp*IrCl2)2;(PENTAMETHYLCYCLOPENTADIENYL)IRIDIUM(III) CHLORIDE DIMER;Dichloro(pentaMethylcyclopentadienyl)iridiuM(III)diMMer;Pentamethylcyclopentadienyliridium(Ⅲ) chloride dimer;PentaMethylcyclopentadienyl)iridiuM(III) chloride diMer,(Cp*IrCl2)2;PentaMethylcyclopentadienyliridiuM(Ⅲ) chloride diMer, 48% Ir, Product of UMicore;PentaMethylcyclopentadienyliridiuM(III) chloride,diMer 96%
CAS:12354-84-6
MF:C20H30Cl4Ir210*
MW:796.7
EINECS:
Product Categories:Ir;organometallic complexes;Catalysts for Organic Synthesis;Classes of Metal Compounds;Homogeneous Catalysts;Ir (Iridium) Compounds;Metal Complexes;Synthetic Organic Chemistry;Transition Metal Compounds;Catalysis and Inorganic Chemistry;Chemical Synthesis;Iridium
Mol File:12354-84-6.mol
(Pentamethylcyclopentadienyl)iridium(III) chloride dimer Structure
(Pentamethylcyclopentadienyl)iridium(III) chloride dimer Chemical Properties
Melting point 245 °C (decomp)(Solv: chloroform (67-66-3); hexane (110-54-3))
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Sparingly), Methanol (Slightly)
form crystal
color orange
Stability:Moisture Sensitive
CAS DataBase Reference12354-84-6
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-R36/37/38
Safety Statements 37/39-26-S37/39-S26-24/25
WGK Germany 3
TSCA No
HS Code 28439000
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
(Pentamethylcyclopentadienyl)iridium(III) chloride dimer Usage And Synthesis
Reaction
  1. Iridium-catalyzed C-3 alkylation of oxindole with alcohols.
  2. Precursor to N-heterocyclic carbene catalyst effective for hydrogenation and alkylation of amines and alcohols.
  3. Precursor to efficient phosphine free catalyst for enantioselective hydrogenation of quinoline derivatives.
  4. Catalyst for oxidative C–H activation.
  5. Precursor to an effective water oxidation catalyst. 
Reactions of 12354-84-6
Chemical Propertiesorange fine crystalline powder
UsesDichloro(pentamethylcyclopentadienyl)iridium(III) dimer is used as a precursor to catalysts for the asymmetric transfer hydrogenation of ketones. It is a catalyst for greener amine synthesis.
General DescriptionThis product has been enhanced for catalytic efficiency.
(Pentamethylcyclopentadienyl)iridium(III) chloride dimer Preparation Products And Raw materials
Bis[(pentamethylcyclopentadienyl)dichloro-rhodium] ALKYLKETENE DIMER BENZAL CHLORIDE (Pentamethylcyclopentadienyl)iridium(III) chloride dimer 2-Chloro-5-chloromethylpyridine SODIUM CYCLOPENTADIENIDE Dichloromethylphenylsilane Dichloroacetic acid Iridium(III) chloride hydrate alpha,alpha'-Dichloro-p-xylene 1,2,3,4,5-Pentamethylcyclopentadiene Tetraphenylcyclopentadienone Iridium Dichlorodimethylsilane METHYLCYCLOPENTADIENE DIMER 2-​[[(2-​ethylphenyl)​(2-​hydroxyethyl)​amino]​methyl]​-​3,​3-​difluoro-Propanenitrile DILINOLEIC ACID 1,3-Cyclopentadiene

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