30358-01-1

Basic information

• Product Name: 4,6-dimethoxy-N-phenyl-1,3,5-triazin-2-amine
• Synonyms: N2-phenyl-4,6-dimethoxy-1,3,5-triazin-2-amine
• CAS NO: 30358-01-1
• Molecular Formula: C₁₁H₁₂N₄O₂
• Molecular Weight: 232.2386
• Mol File: 30358-01-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 397.2°C at 760 mmHg
• Flash Point: 194°C
• Density: 1.268g/cm³
• Vapor Pressure: 1.62E-06mmHg at 25°C
• Refractive Index: 1.607
• CAS DataBase Reference: 4,6-dimethoxy-N-phenyl-1,3,5-triazin-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-dimethoxy-N-phenyl-1,3,5-triazin-2-amine(30358-01-1)
• EPA Substance Registry System: 4,6-dimethoxy-N-phenyl-1,3,5-triazin-2-amine(30358-01-1)

Safety Data

• Hazardous Substances Data: 30358-01-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 2272-40-4 2-phenylamino-4,6-dichloro-s-triazine 
• 62-53-3 aniline 
• 58190-03-7 2-hydroxyamino-4,6-dimethoxy-sym-triazine 
• 3140-73-6 2-chloro-4,6-dimethoxy-1 ,3,5-triazine 

Downstream Products

• 13413-30-4 2,4-di-n-butoxy-6-phenylamino-1,3,5-triazine 

Relevant articles and documents

Zinc base assisted amination of 2-chloropyrimidines by aniline derivatives at room temperature

The amination of 2-chloropyrimidines was performed with several aniline derivatives in the presence of tolylzinc bromide as a base. The organozinc compound has a profound effect on the reactivity of the amines, so that the reaction takes place at room tem

Synthesis, structure, and dynamic behavior in solution of arylamino-1,3,5-triazines. 1. Unsymmetrically substituted arylamino-1,3,5- triazines

Ten unsymmetrically substituted arylamino-1,3,5-triazines were synthesized and studied by dynamic NMR spectroscopy. The free energies of the hindered rotation ΔG≠ are in 59-77 kJ mol-1 range. Using difference-mode NOE NMR experiments

MANGANESE DIOXIDE OXIDATION OF HYDROXYAMINO-sym-TRIAZINES

The hydroxyamino group in sym-triazines is readily oxidized by the action of manganese dioxide.The stability of the nitrosotriazines formed in this oxidation depends on the electron donor properties of the other substituents in the molecule.