BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER

BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER Basic information
Product Name:BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER
Synonyms:Chlorobis(cyclooctene)iridium(I) dimer, Ir nominally 42.9%;Chlorobis(cyclooctene)iridium dimer;Chlorobis(cyclooctene)iridium(Ⅰ) dimer;Chlorobis(cyclooctene)iridiuM(Ⅰ) diMer, 43% Ir, Product of UMicore;Chlorobis(cyclooctene)iridium(I)dimer 97%;Di-μ-chloro(tetramethyl)diiridium - (1Z)-cyclooctene (1:4);Chlorobis(cyclooctene)iridium(I);CHLOROBIS(CYCLOOCTENE)IRIDIUM (I) DIMER
CAS:12246-51-4
MF:C32H56Cl2Ir28*
MW:896.13
EINECS:
Product Categories:Ir;organometallic complex
Mol File:12246-51-4.mol
BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER Structure
BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER Chemical Properties
Melting point 160-165 °C (dec.) (lit.)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Soluble in organic solvents.
form crystal
color yellow
Sensitive moisture sensitive, store cold
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
TSCA No
HS Code 28439000
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER Usage And Synthesis
Chemical PropertiesYellow solid
UsesChlorobis(cyclooctene)iridium(I) dime is used as catalyst for Isomerization-hydroboration reactions with nido-carboranyldiphosphine as stabilizing ligand, Hydrogen peroxide oxidation of hydroxamic acids and their subsequent hetero Diels-Alder cycloaddition reactions, Immobilization of organic functional groups onto solid supports through vinylsilane coupling reactions, Alkylation reactions, Guerbet reaction, Allylic amination reactions in a DNA-diene-iridium(I) hybrid system, Asymmetric hydroamination reactions.
BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER Preparation Products And Raw materials
cis-Cyclooctene BIS(CYCLOOCTENE)IRIDIUM(I) CHLORIDE, DIMER Iridium

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