Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

901116

Sigma-Aldrich

trans-Bis(dicyclohexylphenylphosphine)(2-methylphenyl)nickel(II) chloride

Synonym(s):

trans-(PCy2Ph)2Ni(o-tolyl)Cl

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C43H61ClNiP2
CAS Number:
1419179-26-2
Molecular Weight:
734.04
UNSPSC Code:
12352200

form

powder or solid

reaction suitability

core: nickel
reaction type: Cross Couplings
reagent type: catalyst

mp

174-179 °C

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

Other Notes

Legal Information

Patent application PCT/US2014/064565. Sold under license from the Massachusetts Institute of Technology.

Storage Class Code

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:

Certificates of Analysis (COA)

Lot/Batch Number
MKCF3680

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Recent advances in homogeneous nickel catalysis.
Tasker S Z
Nature, 509(7500), 299-299 (2014)
Simplifying nickel (0) catalysis: an air-stable nickel precatalyst for the internally selective benzylation of terminal alkenes.
Standley E A and Jamison T F
Journal of the American Chemical Society, 135(4), 1585-1592 (2013)
Sarah Z Tasker et al.
Nature, 509(7500), 299-309 (2014-05-16)
Tremendous advances have been made in nickel catalysis over the past decade. Several key properties of nickel, such as facile oxidative addition and ready access to multiple oxidation states, have allowed the development of a broad range of innovative reactions.

Articles

Jamison Nickel (II) Precatalysts

The Jamison group has developed a library of bench-stable phosphine-containing nickel(II) precatalysts that are converted into active catalysts in situ.

Related Content

Jamison Group – Professor Product Portal

Research in the Jamison group is centered on the development of new reactions and technologies for organic synthesis. Towards these themes, the group has pioneered a number of air-stable nickel precatalysts supported by phosphines and N-heterocyclic carbenes that are readily converted to the active catalyst in situ.

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