153998-83-5

Basic information

• Product Name: N¹-(2,6-diisopropylphenyl)benzamidine
• Synonyms: N¹-(2,6-diisopropylphenyl)benzamidine
• CAS NO: 153998-83-5
• Molecular Weight: 280.413
• Mol File: 153998-83-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N¹-(2,6-diisopropylphenyl)benzamidine(CAS DataBase Reference)
• NIST Chemistry Reference: N¹-(2,6-diisopropylphenyl)benzamidine(153998-83-5)
• EPA Substance Registry System: N¹-(2,6-diisopropylphenyl)benzamidine(153998-83-5)

Safety Data

• Hazardous Substances Data: 153998-83-5(Hazardous Substances Data)

Upstream product

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

Downstream Products

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

Relevant articles and documents

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

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).

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.