1129711-31-4

Basic information

• Product Name: 1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)-4,5-dihydro-1H-imidazol-3-ium-chloride
• Synonyms: 1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)-4,5-dihydro-1H-imidazol-3-ium-chloride
• CAS NO: 1129711-31-4
• Molecular Weight: 625.338
• Mol File: 1129711-31-4.mol

Chemical Properties

• CAS DataBase Reference: 1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)-4,5-dihydro-1H-imidazol-3-ium-chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)-4,5-dihydro-1H-imidazol-3-ium-chloride(1129711-31-4)
• EPA Substance Registry System: 1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)-4,5-dihydro-1H-imidazol-3-ium-chloride(1129711-31-4)

Safety Data

• Hazardous Substances Data: 1129711-31-4(Hazardous Substances Data)

Upstream product

• 1129711-19-8 N,N'-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)ethylenediimine 
• 86519-33-7 2,6-diisopropyl-4-(morpholinomethyl)aniline 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 1129711-25-6 N,N'-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)ethylenediamine 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 1129711-37-0 1,3-bis(2,6-diisopropyl-4-(chloromethyl)phenyl)-4,5-dihydro-1-H-imidazol-3-ium chloride 
• 1426223-32-6 (1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)imidazolidin-2-ylidene)copper(I) chloride 
• 1426223-30-4 (1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)imidazolidin-2-ylidene)copper(I) bromide 
• 1426223-31-5 (1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)imidazolidin-2-ylidene)copper(I) iodide 
• 1426223-33-7 (1,3-bis(2,6-diisopropyl-4-(morpholinomethyl)phenyl)imidazolidin-2-ylidene)copper(I) chloride 

Relevant articles and documents

PH-Responsive N-heterocyclic carbene copper(i) complexes: Syntheses and recoverable applications in the carboxylation of arylboronic esters and benzoxazole with carbon dioxide

A pH-controlled monophasic/biphasic switchable system has been developed as a green and novel strategy for homogeneous catalyst recycling, which has been successfully applied to the Cu-NHC-catalyzed carboxylation of organoboronic esters and benzoxazole with carbon dioxide. Additionally, the present strategy could also be extended to the Ag-NHC-catalyzed carboxylation of terminal alkyne. The tertiary amine-functionalized catalysts could be used for at least four times with a slight loss of activity.

Fluorophore tagged cross-coupling catalysts

Fluorophore tagged N-heterocyclic carbenes and the derived (NHC)Pd(allyl)Cl complexes were synthesized and the fluorescence signal was used to follow the course of a Suzuki coupling reaction. The Royal Society of Chemistry.