1917-44-8

Basic information

• Product Name: 1,3,5-Triazin-2(1H)-one, 4,6-diphenyl-
• Synonyms: 1,3,5-Triazin-2(1H)-one, 4,6-diphenyl-;4,6-Diphenyl-1,3,5-triazin-2(1H)-one;Nsc288740;S-Triazin-2(1H)-one, 4,6-diphenyl-;2,4-Diphenyl-6-hydroxy-1,3,5-triazine;2-Hydroxy-4,6-diphenyl-s-triazine;4,6-diphenyl-1H-[1,3,5]triazin-2-one
• CAS NO: 1917-44-8
• Molecular Formula: C₁₅H₁₁N₃O
• Molecular Weight: 249.27
• Mol File: 1917-44-8.mol
• Article Data: 10

Chemical Properties

• Melting Point: 294-295℃
• Boiling Point: 391.1 °C at 760 mmHg
• Flash Point: 190.4 °C
• Appearance: /
• Density: 1.24
• Vapor Pressure: 2.52E-06mmHg at 25°C
• Refractive Index: 1.662
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 6.87±0.70(Predicted)
• CAS DataBase Reference: 1,3,5-Triazin-2(1H)-one, 4,6-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Triazin-2(1H)-one, 4,6-diphenyl-(1917-44-8)
• EPA Substance Registry System: 1,3,5-Triazin-2(1H)-one, 4,6-diphenyl-(1917-44-8)

Safety Data

• Hazardous Substances Data: 1917-44-8(Hazardous Substances Data)

Usage

General Description

1,3,5-Triazin-2(1H)-one, 4,6-diphenyl- is a chemical compound with the molecular formula C15H10N4O. It is a heterocyclic compound consisting of a triazine ring with two phenyl groups attached at the 4 and 6 positions. 1,3,5-Triazin-2(1H)-one, 4,6-diphenyl- has potential applications in the field of organic synthesis and material science, as well as in the development of pharmaceuticals and agrochemicals. It may also be used as a building block in the synthesis of various biologically active compounds. Its unique structure and properties make it a valuable intermediate in the production of a wide range of chemical products.

InChI:InChI=1/C15H11N3O/c19-15-17-13(11-7-3-1-4-8-11)16-14(18-15)12-9-5-2-6-10-12/h1-10H,(H,16,17,18,19)

Upstream product

• 1670-14-0 benzamidine monohydrochloride 
• 57-13-6 urea 
• 75119-49-2 methyl N-(1,2,2,2-tetrachloro-1-phenylethyl)carbamate 
• 100-47-0 benzonitrile 
• 3842-55-5 2-chloro-4,6-diphenyl-1,3,5-triazine 
• 1208-05-5 3-phenyl-5-(trichloromethyl)-1,2,4-oxadiazole 
• 78414-65-0 NN'-dimethyl-N'-(3-phenyl-1,2,4-oxadiazol-5-yl)formohydrazide 
• 78414-68-3 1,1-dimethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)hydrazine 
• 78414-66-1 1-methyl-1-(3-phenyl-1,2,4-oxadiazol-5-yl)hydrazine 
• 7627-10-3 3-phenyl-1,2,4-oxadiazol-5-ylhydrazine 
• 78414-67-2 1,2-dimethyl-1-(3-phenyl-1,2,4-oxadiazol-5-yl)hydrazine 
• 78414-69-4 1,1,2-trimethyl-2-(3-phenyl-1,2,4-oxadiazol-5-yl)hydrazine 
• 66130-09-4 N-(α-aminobenzylidene)-N'-methylurea 
• 100-52-7 benzaldehyde 

Downstream Products

• 3842-55-5 2-chloro-4,6-diphenyl-1,3,5-triazine 
• 6153-86-2 2-chloro-1,3,5-triazine 
• 108784-60-7 1-Benzoyl-4,6-diphenyl-1,3,5-triazin-2-on 

Relevant articles and documents

Preparation method of diaryl-substituted chlorotriazine OLED intermediate

The invention provides a preparation method of a diaryl-substituted chlorotriazine OLED intermediate, and the method comprises the following steps: S1, carrying out heating reaction on an aryl nitrile compound and urea in an organic solvent under the action of strong alkali, and carrying out intermolecular ring closing to form a diaryl hydroxyl triazine compound; S2, enabling the diaryl hydroxyl triazine compound obtained in the step S1 to be subjected to a reaction under the action of phosphorus oxychloride, and obtaining the diaryl chlorinated triazine compound. According to the method, the final product can be obtained only through two-step reaction, raw materials are cheap, and expensive catalysts are not needed. The method has the characteristics of low cost, few steps, high yield, few three wastes, easiness in operation, environment friendliness, suitability for industrialization and the like.

Method for synthesizing 1, 3, 5-triazine derivative

The invention relates to a method for synthesizing a 1, 3, 5-triazine derivative, which is used for synthesizing a 1, 3, 5-triazinone compound and a 2, 4, 6-trisubstituted-1, 3, 5-triazine compound containing three different substituent groups. Synthesis of the 1, 3, 5-triazinone compound comprises the following steps: taking amide, oxalyl chloride and amidine as reaction substrates, and heating for reaction; the synthesis method of the 2, 4, 6-trisubstituted-1, 3, 5-triazine compound containing three different substituent groups comprises the following synthesis steps: by taking amide, oxalyl chloride and amidine as reaction substrates, heating and reacting to obtain a 1, 3, 5-triazinone compound; reacting the 1, 3, 5-triazinone compound, phosphorus oxychloride and triethylamine in acetonitrile to generate a 2-chloro-4, 6-disubstituted 1, 3, 5-triazine compound; and coupling the 2-chloro-4, 6-disubstituted 1, 3, 5-triazine compound with various nucleophilic reagents, so that the 2, 4, 6-trisubstituted-1, 3, 5-triazine compound containing three different substituent groups is prepared. The method is wide in application range and relatively high in reaction yield, provides a new way for synthesis of the 1, 3, 5-triazine derivative, and has a relatively strong industrial application prospect.

Triazine compound

PROBLEM TO BE SOLVED: To provide a novel triazine compound useful as an agent for arylmethylating a nucleophilic compound. SOLUTION: This invention relates to a compound represented by formula (I) [where each symbol is as defined in the specification], an