Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

662232

Sigma-Aldrich

N-Heterocyclic Carbene Ligands Kit I

Synonym(s):

Heterocyclic Carbene Ligands

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
12350000
NACRES:
NA.22

reaction suitability

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst

Quality Level

Kit Components Also Available Separately

Product No.
Description
SDS

  • 6566231,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride, 97% 1 gSDS

  • 6566311,3-Bis(2,4,6-trimethylphenyl)imidazolinium chloride, 95% 1 gSDS

  • 6600191,3-Diisopropylimidazolium tetrafluoroborate, 96% 1 gSDS

  • 6600351,3-Bis(1-adamantyl)imidazolium tetrafluoroborate, 97% 1 gSDS

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

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

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

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

Visit the Document Library

Articles

A wide range of NHC ligands are commonly available which exhibit high activities.

Rapid progress in cross-coupling reactions of unactivated substrates catalyzed by metal complexes has transformed the chemical market-place through introduction of an extensive library of achiral and chiral phosphine ligands.

In collaboration with Umicore AG and Co.,1 we are pleased to offer a series of robust Pd(II) and Pd(0) complexes employed as the linchpin in C–C bond forming reactions.

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