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1,3,5-Triazinane-1,3,5-triyltris(phenylmethanone), also known as triazine-triyltris-benzophenone, is a complex organic compound with the chemical formula C27H15N3O3. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. 1,3,5-triazinane-1,3,5-triyltris(phenylmethanone) is characterized by a triazine ring with three benzophenone groups attached to it, forming a rigid, planar structure. It is often used as a photostabilizer in polymers and coatings due to its ability to absorb ultraviolet light and prevent the degradation of materials under exposure to sunlight. The compound's stability and effectiveness in protecting against UV radiation make it a valuable additive in various industrial applications, such as in the production of plastics, paints, and adhesives.

5434-82-2

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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.

5434-82-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,5-dibenzoyl-1,3,5-triazinan-1-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 1,3,5-tribenzoylperhydro-1,3,5-triazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5434-82-2 SDS

5434-82-2Relevant academic research and scientific papers

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.

Synthesis of 1,3,5-Triacylperhydro-1,3,5-triazines Catalyzed by Ion-Exchange Resins

Ladhar, F.,El Gharbi, R.,Delmas, M.,Gaset, A.

, p. 643 - 644 (2007/10/02)

1,3,5-Triacylperhydro-1,3,5-triazines can be obtained in high yields by reaction of 1,3,5-trioxan with nitriles in solvents such as chlorobenzene using as catalyst an ion-exchange resin such as Amberlyst 15 with precise control of the hydration rate of the resin.

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.

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