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About This Item
Empirical Formula (Hill Notation):
C20H30Cl4Ir2
CAS Number:
Molecular Weight:
796.70
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Product Name
Pentamethylcyclopentadienyliridium(III) chloride,dimer, 96%
Quality Segment
assay
96%
form
solid
reaction suitability
core: iridium, reagent type: catalyst
sustainability
Sustainability features
SMILES string
Cl[Ir]Cl.Cl[Ir]Cl.C[C]1[C](C)[C](C)[C](C)[C]1C.C[C]2[C](C)[C](C)[C](C)[C]2C
InChI
1S/2C10H15.4ClH.2Ir/c2*1-6-7(2)9(4)10(5)8(6)3;;;;;;/h2*1-5H3;4*1H;;/q;;;;;;2*+2/p-4
InChI key
JDOHSXHCQARCAW-UHFFFAOYSA-J
General description
Pentamethylcyclopentadienyliridium(III) chloride, dimer is utilized as a catalyst in cross-coupling and dimerization reactions.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
Application
Catalyst for greener amine synthesis from amines and alcohols by hydrogen-borrowing. Precursor to cooperative metal-Bronsted acid catalyst for greener reductive amination using hydrogen gas.
Metal-Brønsted Acid Cooperative Catalysis for Asymmetric Reductive Amination
Development of GSK's reagent guides – embedding sustainability into reagent selection
Metal-Brønsted Acid Cooperative Catalysis for Asymmetric Reductive Amination
Development of GSK's reagent guides – embedding sustainability into reagent selection
Storage Class
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
PPE (personal protective equipment)
Eyeshields, Gloves, type N95 (US)
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