ChemicalBook > Product Catalog > Organic Chemistry > Organometallic compounds > Organic iridium > (Pentamethylcyclopentadienyl)iridium(III) chloride dimer
(Pentamethylcyclopentadienyl)iridium(III) chloride dimer
(Pentamethylcyclopentadienyl)iridium(III) chloride dimer Basic information
- 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
- 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
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(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 Reference
- 12354-84-6
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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
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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(Pentamethylcyclopentadienyl)iridium(III) chloride dimer Usage And Synthesis
Reaction
- Iridium-catalyzed C-3 alkylation of oxindole with alcohols.
- Precursor to N-heterocyclic carbene catalyst effective for hydrogenation and alkylation of amines and alcohols.
- Precursor to efficient phosphine free catalyst for enantioselective hydrogenation of quinoline derivatives.
- Catalyst for oxidative C–H activation.
- Precursor to an effective water oxidation catalyst.
Chemical Properties
orange fine crystalline powder
Uses
Dichloro(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 Description
This product has been enhanced for catalytic efficiency.
(Pentamethylcyclopentadienyl)iridium(III) chloride dimerSupplier
Shaanxi Rock New Materials Co., Ltd. Gold
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J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
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(Pentamethylcyclopentadienyl)iridium(III) chloride dimer(12354-84-6)Related Product Information
- METHYLCYCLOPENTADIENE DIMER
- Sodium chloride
- alpha,alpha'-Dichloro-p-xylene
- Tetraphenylcyclopentadienone
- Dichloromethylphenylsilane
- 1,2,3,4,5-Pentamethylcyclopentadiene
- Dichloroacetic acid
- DILINOLEIC ACID
- SODIUM CYCLOPENTADIENIDE
- 1,3-Cyclopentadiene
- Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]
- Iridium
- 2-Chloro-5-chloromethylpyridine
- Dichlorodimethylsilane
- BENZAL CHLORIDE
- Iridium(III) chloride hydrate
- (Pentamethylcyclopentadienyl)iridium(III) chloride dimer
- ALKYLKETENE DIMER