14117-12-5

Basic information

• Product Name: 2,4,6-tris(3,4-dimethylphenyl )-1,3,5-triazine
• Synonyms: 2,4,6-tris(3,4-dimethylphenyl )-1,3,5-triazine
• CAS NO: 14117-12-5
• Molecular Weight: 393.531
• Mol File: 14117-12-5.mol

Chemical Properties

• CAS DataBase Reference: 2,4,6-tris(3,4-dimethylphenyl )-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(3,4-dimethylphenyl )-1,3,5-triazine(14117-12-5)
• EPA Substance Registry System: 2,4,6-tris(3,4-dimethylphenyl )-1,3,5-triazine(14117-12-5)

Safety Data

• Hazardous Substances Data: 14117-12-5(Hazardous Substances Data)

Upstream product

• 14921-00-7 cyanuric bromide 
• 95-47-6 o-xylene 
• 5973-71-7 3,4-dimethylbenzaldehyde 
• 506-68-3 bromocyane 

Downstream Products

• 619-04-5 3,4-dimethylbenzoic acid 

Relevant articles and documents

Method for synthesizing 2, 4, 6-trisubstituted 1, 3, 5-triazine compound from aromatic aldehyde and ammonium iodide

The invention discloses a method for synthesizing a 2, 4, 6-trisubstituted 1, 3, 5-triazine compound from aromatic aldehyde and ammonium iodide, and belongs to the field of organic synthesis. According to the method, aromatic aldehyde and ammonium iodide undergo a one-pot reaction under the catalytic action of a ferric salt, so that the 2, 4, 6-trisubstituted 1, 3, 5-triazine compound is obtained.According to the present invention, the small molecule aryl aldehyde raw material and the iron salt catalyst are used, such that the cost is low, the reaction conditions are mild, the symmetric 2, 4,6-trisubstituted 1, 3, 5-triazine compound can be highly selectively obtained, and the brand-new synthesis idea is provided for the triazine ring construction.

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.

S-Triazine hexacarboxylic acids and trianhydrides

s-Triazine hexacarboxylic acids having the formula SPC1 Can be prepared by reacting cyanuric chloride with a diakyl substituted aromatic compound and thereafter oxidizing the intermediate to yield the above acid. By dehydrating the acid a corresponding trianhydride is obtained. Such compounds are useful as crosslinking agents for resin systems.