1596320-79-4

Basic information

• Product Name: 2,4-di-phenyl-6-(pyridin-3-yl)-1,3,5-triazine
• Synonyms: 2,4-di-phenyl-6-(pyridin-3-yl)-1,3,5-triazine
• CAS NO: 1596320-79-4
• Molecular Weight: 310.358
• Mol File: 1596320-79-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,4-di-phenyl-6-(pyridin-3-yl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-di-phenyl-6-(pyridin-3-yl)-1,3,5-triazine(1596320-79-4)
• EPA Substance Registry System: 2,4-di-phenyl-6-(pyridin-3-yl)-1,3,5-triazine(1596320-79-4)

Safety Data

• Hazardous Substances Data: 1596320-79-4(Hazardous Substances Data)

Upstream product

• 3731-52-0 3-Aminomethylpyridine 
• 1670-14-0 benzamidine monohydrochloride 
• 350-03-8 methyl-3-pyridylketone 
• 100-55-0 3-hydroxymethylpyridin 

Relevant articles and documents

Polythene glycol (PEG) as a reusable solvent system for the synthesis of 1,3,5-triazines via aerobic oxidative tandem cyclization of benzylamines and N-substituted benzylamines with amidines under transition metal-free conditions

A green and highly efficient protocol for the synthesis of 1,3,5-triazines from benzylamines and N-substituted benzylamines with amidines in PEG-600 has been developed. This protocol is transition-metal free, phosphine ligand free and uses inexpensive, easily available molecular oxygen (O2) as an oxidant. A series of 1,3,5-triazines derivatives were synthesized in good to excellent yields in a shorter reaction time. The ease of the product separation and reusability of PEG-600 makes it more environmentally benign and economically affordable for gram-scale synthesis.

Iridium-catalyzed cascade dehydrogenation, ring-closure reaction leading to 2,4,6-triaryl-1,3,5-triazines

An efficient iridium-catalyzed dehydrogenation, ring-closure reaction, has been developed via a cascade sequence, in which [Cp?IrI2]2/Xantphos proved to be the most efficient catalyst for the synthesis of 2,4,6-triaryl-1,3,5-triazines from stable aryl-substituted alcohols and amidines. It was the first case of iridium catalyst successful application in such transformation.

NIS-catalyzed oxidative cyclization of alcohols with amidines: A simple and efficient transition-metal free method for the synthesis of 1,3,5-triazines

An efficient method for the synthesis of 1,3,5-triazines by NIS-catalyzed oxidative cyclization of alcohols with amidines has been developed. The reaction works smoothly under transition-metal free and phosphine-free conditions to afford a wide range of 1,3,5-triazine derivatives in moderate to good yields. The synthetic methodology was achieved via in situ oxidation of alcohols to aldehydes.