377155
Chlorobis(cyclooctene)iridium(I)dimer
97%
Sinónimos:
[Ir(coe)2Cl]2, Di-μ-chlorotetrakis(cyclooctene)diiridium
About This Item
Productos recomendados
Quality Level
assay
97%
form
powder
reaction suitability
core: iridium
reagent type: catalyst
mp
160-165 °C (dec.) (lit.)
SMILES string
Cl[Ir].Cl[Ir].[CH]1[CH]CCCCCC1.[CH]2[CH]CCCCCC2.[CH]3[CH]CCCCCC3.[CH]4[CH]CCCCCC4
InChI
1S/4C8H14.2ClH.2Ir/c4*1-2-4-6-8-7-5-3-1;;;;/h4*1-2H,3-8H2;2*1H;;/q;;;;;;2*+1/p-2/b4*2-1-;;;;
InChI key
WBRREXQCZAFSKS-XFCUKONHSA-L
Categorías relacionadas
Application
- 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
- 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 using a DNA-diene-iridium(I) hybrid system.
- Asymmetric hydroamination reactions.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Artículos
Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.
Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.
Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.
Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.
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