901116
trans-Bis(dicyclohexylphenylphosphine)(2-methylphenyl)nickel(II) chloride
Synonym(s):
trans-(PCy2Ph)2Ni(o-tolyl)Cl
Select a Size
About This Item
SMILES string
Cl[Ni](P(C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H])(C2=C([H])C([H])=C([H])C([H])=C2[H])C3([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C3([H])[H])(P(C4([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C4([H])[H])(C5=C([H])C([H])=C([H
form
powder or solid
reaction suitability
core: nickel, reaction type: Cross Couplings, reagent type: catalyst
mp
174-179 °C
Other Notes
Legal Information
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
The Jamison group has developed a library of bench-stable phosphine-containing nickel(II) precatalysts that are converted into active catalysts in situ.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Related Content
Jamison group focuses on new reaction development for organic synthesis, pioneering air-stable nickel precatalysts.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service