1620330-18-8

Basic information

• Product Name: 2,4,6-tris(4-ethylphenyl)-1,3,5-triazine
• Synonyms: 2,4,6-tris(4-ethylphenyl)-1,3,5-triazine
• CAS NO: 1620330-18-8
• Molecular Weight: 393.531
• Mol File: 1620330-18-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,4,6-tris(4-ethylphenyl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(4-ethylphenyl)-1,3,5-triazine(1620330-18-8)
• EPA Substance Registry System: 2,4,6-tris(4-ethylphenyl)-1,3,5-triazine(1620330-18-8)

Safety Data

• Hazardous Substances Data: 1620330-18-8(Hazardous Substances Data)

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 63139-21-9 4-ethylphenylboronic acid 
• 4748-78-1 4-ethylbenzylaldehyde 
• 25309-65-3 4-ethylbenzonitrile 
• 1620330-24-6 C₁₀H₉F₃NO₂S⁽¹⁺⁾*CF₃O₃S^(1-) 

Relevant articles and documents

Sustainable and recyclable magnetic nanocatalyst of 1,10-phenanthroline Pd(0) complex in green synthesis of biaryls and tetrazoles using arylboronic acids as versatile substrates

A magnetic nanocatalyst was purveyed as a heterogeneous recoverable palladium-based catalyst anchored on green, sustainable and phosphine free support. Resulted Fe3O4@SiO2-Phen-Pd(0) nanocatalyst bearing powerful phenanthroline ligand was thoroughly characterized by physicochemical approaches like UV–vis, FT-IR, EDX, XRD, TGA, ICP, VSM, DLS, FESEM, and TEM analyses. After finding trustable data, the obtained magnetic catalyst was considered to be applied in the Suzuki-Miyaura type C-C couplings and getting corresponding tetrazoles using arylboronic acid derivatives as alternate precursors of aromatic halides and stupendous data were observed.

Atom-efficient synthesis of 2,4,6-trisubstituted 1,3,5-triazinesviaFe-catalyzed cyclization of aldehydes with NH4I as the sole nitrogen source

An atom-efficient, straightforward method for the synthesis of 2,4,6-triaryl-1,3,5-triazinesviairon-catalyzed cyclization of aldehydes with NH4I as the sole nitrogen source is demonstrated. This strategy works smoothly under air atmosphere, and affords symmetrical 2,4,6-trisubstituted and unsymmetrical 1,3,5-triazines with yields from 18% to 72%. Compared to other methods, the present protocol provides a straightforward and atom-efficient approach to 2,4,6-trisubstituted 1,3,5-triazines using an inexpensive, easily available ammonium salt as the sole nitrogen source. Research into the preliminary mechanism indicates thatN-benzylidenebenzimidamides are involved in this cyclization reaction.