683094
HS157
Umicore, 97%
Synonym(s):
Bis(1,5-cyclooctadiene)diiridium(I) dichloride, [Ir(1,5-cod)Cl]2, 1,5-Cyclooctadiene-iridium(I) chloride dimer, Chloro(1,5-cyclooctadiene)iridium(I) dimer, Di-μ-chlorobis[(1,2,5,6-η)-1,5-cyclooctadiene]diiridium, Iridium(I) chloride 1,5-cyclooctadiene complex dimer, [Ir(1,5-cod)Cl]2, [Ir(cod)Cl]2
About This Item
Quality Level
assay
97%
form
powder
reaction suitability
core: iridium
reaction type: C-H Activation
reagent type: catalyst
mp
205 °C (dec.) (lit.)
SMILES string
Cl[Ir].Cl[Ir].C1CC=CCCC=C1.C2CC=CCCC=C2
InChI
1S/2C8H12.2ClH.2Ir/c2*1-2-4-6-8-7-5-3-1;;;;/h2*1-2,7-8H,3-6H2;2*1H;;/q;;;;2*+1/p-2/b2*2-1-,8-7-;;;;
InChI key
ZFOUDQNHNLDNLD-MIXQCLKLSA-L
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Related Categories
Application
Metal precursor for asymmetric allylic substitutions.
Legal Information
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
Certificates of Analysis (COA)
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Articles
Arylboronic acids and esters are invaluable tools for the chemical community. These powerful reagents are used for a variety of transformations, most notably the Suzuki-Miyaura cross-coupling reaction.
We are happy to offer a series of precatalysts for asymmetric catalysis and Pd based cross coupling catalysis. Our partnership with Umicore allows us to offer a portfolio of metal complexes with batch-to-batch consistency for a plethora of catalytic reactions.
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