153998-83-5

Upstream product

• 24544-04-5 2,6-diisopropylbenzenamine 
• 100-47-0 benzonitrile 
• 55-21-0 benzamide 

Downstream Products

• 1278597-81-1 N-[(2,6-diisopropylphenylamino)phenylmethylene]-2,2,-dimethylpropionamide 
• 1352641-91-8 [(N(2,6-diisopropylphenyl)benzamidine)AlCl₃] 
• 1439365-20-4 1,5-bis(2,6-diisopropylphenyl)-2,4-diphenyl-1,3,5-triazapenta-1,3-diene 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 100-47-0 benzonitrile 
• 914306-50-6 1-(2,6-diisopropylphenyl)-2-phenyl-1H-imidazole 

Relevant academic research and scientific papers

Calcium mediated efficient synthesis ofN-arylamidines from organic nitriles and amines

Amidines are a preeminent group of organic compounds having wide applications in various industries. Here, we have developed a simple one-step reaction protocol for the facile synthesis ofN-arylamidines catalysed by calcium bis(hexamethyldisilazide) [Ca{N

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

The present invention includes novel hexadentate metal complexes. The complexes hexadentate ligands of the present invention may be useful as improved emitters in an OLED device.

Trimethylaluminium-mediated reaction of primary carboxamides with amines and indoles: A convenient synthesis of amidines and indole-3-acylimines

A simple, convenient and general method, exhibiting good functional group tolerance, is described for the synthesis of N- and N,N-disubstituted amidines by the reaction of primary carboxamides with amines mediated by trimethylaluminium (AlMe3).

Synthesis, characterization of bridged bis(amidinate) lanthanide amides and their application as catalysts for addition of amines to nitriles for monosubstituted N-arylamidines

A series of lanthanide amide complexes supported by bridged bis(amidinate) ligand L, LLnNHAr1(DME) (L = [Me3SiNC(Ph)N(CH 2)3NC(Ph)NSiMe3], Ar1 = 2,6- iPr2C6

PHOSPHINYL AMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS

N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, N2-phosphinyl amidinate metal salt complexes are described. Methods for making N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes are also disclosed. Catalyst systems utilizing the N2-phosphinyl amidine metal salt complexes and N2-phosphinyl amidinate metal salt complexes are also disclosed along with the use of the N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes for the oligomerization and/or polymerization of olefins.

Synthesis and molecular structures of lanthanocene amide complexes and their catalytic activity for addition of amines to nitriles

Reaction of (CH3C5H4)2LnCl(THF) with NaNHAr in a 1:1 molar ratio in THF afforded the amide complexes (CH3C5H4)2LnNHAr(THF) [(Ar = 2,6-Me2C6H