5434-82-2 Usage
Chemical structure
1,3,5-triazinane-1,3,5-triyltris(phenylmethanone) is a trisubstituted triazine with three phenylmethanone groups attached to the triazine ring.
Functional groups
The compound contains a triazine ring and three phenylmethanone groups.
Molecular weight
Approximately 399.39 g/mol
Appearance
The compound is likely to be a solid, although the exact appearance is not provided in the material.
Applications
It can be used as a building block in organic synthesis and has potential applications in the pharmaceutical and chemical industries.
Synthesis
The compound can be synthesized by reacting a triazine core with three equivalents of a phenylmethanone derivative.
Biological activity
It has been studied for its potential biological activity, making it of interest for further research and development in the field of medicinal chemistry.
Stability
The stability of the compound is not explicitly mentioned in the material, but it is likely to be stable under normal laboratory conditions due to its use as a building block in organic synthesis.
Solubility
The solubility of the compound is not provided in the material, but it may be soluble in common organic solvents such as dichloromethane, acetone, or ethanol, based on the presence of the phenylmethanone groups.
Check Digit Verification of cas no
The CAS Registry Mumber 5434-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5434-82:
(6*5)+(5*4)+(4*3)+(3*4)+(2*8)+(1*2)=92
92 % 10 = 2
So 5434-82-2 is a valid CAS Registry Number.
5434-82-2Relevant articles and documents
Triacylperhydro-1,3,5-triazines over phenylsulfonic acid functionalized mesoporous silica
Yang, Jianming,Yu, Qinwei,Zhao, Fengwei,Lu, Jian,Ge, Zhongxue
experimental part, p. 3455 - 3461 (2011/10/09)
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
Nishiyama, Kozaburo,Mikuni, Hioruki,Harada, Mari
, p. 3381 - 3382 (2007/10/02)
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.
