s-Triazine, 2,4,6-triphenoxy-

Name	2,4,6-Triphenoxy-s-triazine
Synonyms	217-644-5 triphenylcyanurate Triphenyl cyanurate Triphenyl-s-triazine Triphenoxy-s-triazine 2,4,6-triphenoxy-s-triazin 2,4,6-Triphenoxy-s-triazine s-Triazine, 2,4,6-triphenoxy- 5-triazine,2,4,6-triphenoxy-3 2,4,6-Triphenyl-1,3,5-triazine 2,4,6-triphenoxy-1,3,5-triazine 1,3,5-triazine, 2,4,6-triphenyl- 1,3,5-TRIAZINE, 2,4,6-TRIPHENOXY- 2,4,6-Tris-phenoxy-[1,3,5]triazine
CAS	1919-48-8
EINECS	217-644-5
InChI	InChI=1/C21H15N3O3/c1-4-10-16(11-5-1)25-19-22-20(26-17-12-6-2-7-13-17)24-21(23-19)27-18-14-8-3-9-15-18/h1-15H

Risk Codes	22 - Harmful if swallowed
Safety Description	24/25 - Avoid contact with skin and eyes.
WGK Germany	3
RTECS	XZ2030000
TSCA	Yes
HS Code	29336980
Hazard Note	Irritant

EPA chemical information	Information provided by: ofmpub.epa.gov (external link)
use	2,4, 6-triphenoxy -1,3, 5-triazine is also called 2,4, 6-triphenol -1,3, 5-triazine. It belongs to a class of small molecule, branched and polymer materials containing special triazine units. This kind of materials are used in organic electroluminescence, organic field effect tube, organic solar cell, nonlinear optics, biosensing, organic light storage and organic laser and other fields have a wide range of applications.
structural properties	organic photoelectric functional materials such as liquid crystal, nonlinear optics and electroluminescence derived from 1,3, 5-triazine have star-shaped, hyperbranched and dendritic three-dimensional structures. In this class of macromolecules, symmetrically substituted 2,4, 6-triphenoxy -1, 3,5-triazine is a class of basic structural units, and 2,4, 6-triphenoxy -1, 3,5-triazine derivatives containing multiple functional groups are used as functional modules for constructing macromolecular organic optoelectronic functional materials.
preparation	0.5g trichlorotriazine, 0.84g phenol and 0.37g sodium hydroxide solid are added into two bottles, vacuumed and filled with nitrogen, then 30ml of acetone/water (1: 1) mixed solution is added, reacted at 80 ℃ for 24h, and the reaction is finished and filtered and recrystallized directly. The yield is 93%.

Last Update：2024-04-09 20:52:54