46323-27-7

Upstream product

• 4238-71-5 1-benzylimidazole 
• 506-68-3 bromocyane 
• 100-39-0 benzyl bromide 
• 31722-49-3 2-cyano imidazole 
• 506-77-4 cyanogen chloride 
• 59016-54-5 1-cyano-4-N,N-dimethylaminopyridinium bromide 

Downstream Products

• 111851-95-7 1-(phenylmethyl)-4'(5')-methyl-2,2'-bi-1H-imidazole 
• 878649-97-9 1-benzyl-N-hydroxy-1H-imidazole-2-carboxamidine 
• 63927-95-7 5-(1-benzyl-1H-imidazol-2-yl)-1⁽²⁾H-tetrazole 
• 878650-07-8 2-[(1-benzyl-1H-imidazole-2-carboximidoyl)-aminooxy]-but-2-enedioic acid dimethyl ester 
• 878650-18-1 2-(1-benzyl-1H-imidazol-2-yl)-5,6-dihydroxy-pyrimidine-4-carboxylic acid methyl ester 
• 31722-49-3 2-cyano imidazole 

Relevant academic research and scientific papers

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

Disclosed are platinum or palladium complexes featuring tetradentate ligands with at least one side that has an NN binding motif are disclosed. The disclosed organometallic compounds have a structure of where M is Pt or Pd. Also provided are formulations comprising these organometallic compounds. Further provided are OLEDs and related consumer products that utilize these organometallic compounds.

Novel synthesis of heterocyclic aryl amidines

We have developed a novel amidine synthesis that allows the preparation of heterocyclic amidines that were previously unknown and difficult to prepare by published methods. The route involves the lithiation of heterocycles by the action of n-BuLi followed

2,2'-bi-1H-imidazoles

This invention relates to novel derivatives of 2,2'-bi-1H-imidazoles, to the processes and intermediates used in their preparation, to their ability to exert the pharmacologic effects of lowering high blood pressure and of increasing heart contractile force and to their use as chemotherpauetic agents useful in treating cardiac insufficiency and hypertension.

Cyanogen Bromide-Dimethylaminopyridine (CAP): A Convenient Source of Positive Cyanide for the Synthesis of 2-Cyanoimidazoles

Dimethylaminopyridine activates cyanogen bromide towards C-C bond formation by forming 1-cyano-4-dimethylaminopyridinium bromide.The latter serves as a convenient reagent for the synthesis of 2-cyanoimidazoles.

N-CYANO-N'-ALKYLIMIDAZOLIUM YLIDS AS NOVEL INTERMEDIATES TO 2-CYANOIMIDAZOLES

N-Substituted imidazoles were readily converted to 2-cyanoimidazoles by treatment with cyanogen chloride followed by triethylamine.The utilization of the SEM protecting group provided a facile entry to N-unsubstituted 2-cyanoimidazoles.