5434-82-2

Basic information

• Product Name: 1,3,5-triazinane-1,3,5-triyltris(phenylmethanone)
• Synonyms: 1,3,5-Triazine, hexahydro-1,3,5-tribenzoyl-; 1,3,5-Tribenzoyl-1,3,5-triazinane; 1,3,5-TRIBENZOYLHEXAHYDRO-S-TRIAZINE; methanone, 1,1',1''-(1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tris[1-phenyl-
• CAS NO: 5434-82-2
• Molecular Formula: C₂₄H₂₁N₃O₃
• Molecular Weight: 399.4418
• Mol File: 5434-82-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 638.8°C at 760 mmHg
• Flash Point: 296°C
• Density: 1.285g/cm³
• Vapor Pressure: 3.26E-16mmHg at 25°C
• Refractive Index: 1.651
• CAS DataBase Reference: 1,3,5-triazinane-1,3,5-triyltris(phenylmethanone)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-triazinane-1,3,5-triyltris(phenylmethanone)(5434-82-2)
• EPA Substance Registry System: 1,3,5-triazinane-1,3,5-triyltris(phenylmethanone)(5434-82-2)

Safety Data

• Hazardous Substances Data: 5434-82-2(Hazardous Substances Data)

Usage

General Description

1,3,5-triazinane-1,3,5-triyltris(phenylmethanone) is a chemical compound that consists of a triazine ring with three attached phenylmethanone groups. It is a trisubstituted triazine and can be used as a building block in organic synthesis. The compound has potential applications in the pharmaceutical and chemical industries, where it can be used as a precursor for the synthesis of various organic compounds. It has also been studied for its potential biological activity, and its structure and properties make it of interest for further research and development in the field of medicinal chemistry.

Upstream product

• 110-88-3 1,3,5-Trioxan 
• 100-47-0 benzonitrile 
• 50-00-0 formaldehyd 
• 98-88-4 benzoyl chloride 
• 7664-93-9 sulfuric acid 
• 87576-94-1 trimethylsilylmethyl azide 
• 100-97-0 hexamethylenetetramine 

Downstream Products

• 50-00-0 formaldehyd 
• 65-85-0 benzoic acid 
• 116047-00-8 2-deuterio-1,3,5-tribenzoylhexahydro-sym-triazine 

Relevant articles and documents

Triacylperhydro-1,3,5-triazines over phenylsulfonic acid functionalized mesoporous silica

An operationally simple, efficient, and environmentally benign synthesis of 1,3,5-triacylperhydro-1,3,5-triazines in good yields by reaction of different organic nitriles and trioxane in the presence of phenylsulfonic acid functionalized mesoporous silica under mild conditions was examined. The yields of the corresponding 1,3,5-trisubstituted perhydro-s-triazines synthesized from acetonitrile, propionitrile, butyronitrile, benzonitrile, and 1.3.5-trioxane were 95.7%, 96.1%, 84.2%, and 98.1%, respectively. The products were characterized by 1H NMR, infrared, mass spectrometry, and elemental analysis. The mechanism of the formation of 1,3,5-triacylperhydro-1,3,5-triazines in acidic conditions was also described using a model reaction of butyronitrile with trioxane.

Reactions of Trimethylsilylmethyl Azide with Aromatic Acid Derivatives Catalyzed by Fluoride Ion

The treatment of an aromatic acid halide with trimethylsilylmethyl azide (TMSMA) in the presence of potassium fluoride and crown ether gave triazine, methanediamine, and benzamide derivatives, while the reaction of acid anhydride with TMSMA gave tertiary amine together with methanediamine and benzamide under similar conditions.