928797-95-9

Basic information

• Product Name: 2H-Imidazol-2-imine, 1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-
• CAS NO: 928797-95-9
• Molecular Formula: C27H37N3
• Molecular Weight: 403.611
• Mol File: 928797-95-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2H-Imidazol-2-imine, 1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Imidazol-2-imine, 1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-(928797-95-9)
• EPA Substance Registry System: 2H-Imidazol-2-imine, 1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-(928797-95-9)

Safety Data

• Hazardous Substances Data: 928797-95-9(Hazardous Substances Data)

Upstream product

• 917-54-4 methyllithium 
• 244187-81-3 1,3-bis-(2,6-diisopropylphenyl)-imidazol-2-ylidene 
• 250285-32-6 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride 
• 74663-75-5 1,2-bis(2,6-diisopropylphenylimino)ethane 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 4648-54-8 trimethylsilylazide 
• 888854-17-9 1,3-bis(2,6-diisopropylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene 

Relevant articles and documents

Structural and theoretical investigation of 2-iminoimidazolines - Carbene analogues of iminophosphoranes

The preparation of 2-iminoimidazolines 3a-3f has been accomplished by the Staudinger reaction of the carbenes 1,3-di-tert-butylimidazolin-2-ylidene (1a), 1,3-diisopropyl-4,5-dimethylimidazolin-2-ylidene (1b), 1,3- diisopropylimidazolin-2-ylidene (1c), 1,3

Contrasting reactivities of silicon and germanium complexes supported by an N -heterocyclic guanidine ligand

We report the synthesis of an acyclic two-coordinate germylene supported by two bulky and electron donating N-heterocyclic guanidine [IPr=N]- ligands (IPr = [(HCNDipp)2C:]; Dipp = [2,6-iPr2C6H3/

Isolation of Phosphinoimino-2-imidazoline

The phosphinoimino-2-imidazoline 4 was synthesized by a salt elimination reaction between LiNIPr [NIPr = 1,3-bis(2,6-(diisopropylphenyl)imidazolin-2-ylidenamino)] and 2-chloro-1,3,2-diazaphospholene. DFT study revealed that the HOMO of 4 involves the lone pair orbitals on the P atom and the N atom at the exocyclic P–N bond. Compound 4 displays selectivity in coordinating to acids. Thus, the N atom at the exocyclic P–N bond coordinates to a hard acid (HCl) which eventually led to the cleavage of the P–N bond, while the central P atom forms a dative bond with a soft Lewis acid, BH3.