1096001-27-2

Basic information

• Product Name: N,N'-bis(2,6-diisopropylphenyl)-N-formylethylenediamine
• Synonyms: N,N'-bis(2,6-diisopropylphenyl)-N-formylethylenediamine
• CAS NO: 1096001-27-2
• Molecular Weight: 408.627
• Mol File: 1096001-27-2.mol

Chemical Properties

• CAS DataBase Reference: N,N'-bis(2,6-diisopropylphenyl)-N-formylethylenediamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-bis(2,6-diisopropylphenyl)-N-formylethylenediamine(1096001-27-2)
• EPA Substance Registry System: N,N'-bis(2,6-diisopropylphenyl)-N-formylethylenediamine(1096001-27-2)

Safety Data

• Hazardous Substances Data: 1096001-27-2(Hazardous Substances Data)

Upstream product

• 258278-28-3 1,3-bis(2,6-diisopropylphenyl)dihydroimidazol-2-ylidene 
• 103-83-3 N,N'-dimethylbenzylamine 
• 258278-25-0 1,3-bis[(2,6-diisopropyl)phenyl]imidazolinium chloride 

Relevant articles and documents

Practical one-pot, three-component synthesis of N-heterocyclic carbene (NHC) ligated palladacycles derived from n,n-dimethylbenzylamine

Further explorations of the catalytic potential of N-heterocyclic carbene (NHC) ligated palladacycles as catalysts for Pd-mediated transformations have been hampered by the lack of general and practical methods for their synthesis. In this work, we descri

Dioxygen activation with stable N-heterocyclic carbenes

Dioxygen activation with both cyclic (amino)(alkyl)carbenes and di(amino)carbenes at ambient temperature is described. Theoretical studies suggest that electron rearrangement from the doubly filled σ orbital of carbene carbon to its vacant p orbital through the π? antibonding orbital of 3O2 can be considered for Ccarbene-O bond formation.

Dual reactivity of N-heterocyclic carbenes towards copper(ii) salts

Complexes of N-heterocyclic carbenes (NHCs) with copper(ii) halogenides are unstable. Upon formation, these complexes decompose to give haloamidinium salts. Contrastingly, O-substituted copper(ii) NHC complexes are fairly stable. A series of new five-, si