134890-49-6

Basic information

• Product Name: 1,3,5-tri(2,4-dichlorophenyl)-1,3,5-triazine
• Synonyms: 1,3,5-tri(2,4-dichlorophenyl)-1,3,5-triazine
• CAS NO: 134890-49-6
• Molecular Weight: 522.088
• Mol File: 134890-49-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3,5-tri(2,4-dichlorophenyl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tri(2,4-dichlorophenyl)-1,3,5-triazine(134890-49-6)
• EPA Substance Registry System: 1,3,5-tri(2,4-dichlorophenyl)-1,3,5-triazine(134890-49-6)

Safety Data

• Hazardous Substances Data: 134890-49-6(Hazardous Substances Data)

Upstream product

• 112844-22-1 N,N'-bis-(2,4-dichloro-phenyl)-methylenediamine 
• 554-00-7 2,4-Dichloroaniline 
• 50-00-0 formaldehyd 
• 58042-95-8 acide 5,5-diethyl-4-iminobarbiturique 

Relevant articles and documents

Synthesis and study of antimicrobial activities of variously chlorosubstituted 3-phenyloctahydropyrimido-[3,4-a]-s-triazines

These compounds were synthesised, via a double Mannich reaction between 5,5-diethyl-4-iminobarbituric acid, formaldehyde and primary chlorophenylamines. The by-products of the reaction, 1,3,5,-triarylhexahydro-s-triazines and monoamino-methylpyrimidinediones, were identified and their formation discussed. It was shown that the extracyclic nitrogen atom underwent the first aminomethylation and that the substitution of the intracyclic nitrogen atom, inducing ring closure, took place in a second step. All the compounds exhibited antimicrobial activities against bacteria and/or fungi and the derivative presenting a chlorine atom in the 3-position on the nucleus was as active as miconazole nitrate agonist T rubrum and E floccosum.