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CAS:90723-86-7 | 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine

CAS:90723-86-7 | 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine

Molecular Formula:C10H7Cl2N3O
Molecular Weigh:256.09
EINECS:604-604-1
Package:100g 1kg 5kg
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Product Introduction

Introduction of CAS:90723-86-7 | 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine

 

The synthesis of 2,4-Dichloro-6-(4-methoxyphenyl)-1,3,5-triazine has been refined to avoid the problematic Grignard reaction of 4-bromo-anisole. An improved synthesis method has been developed, yielding the pure compound more efficiently. This method facilitates the subsequent preparation of bis(resorcinyl) triazine derivatives, which are potent UV light absorbers, by using 2,4-Dichloro-6-(4-methoxyphenyl)-1,3,5-triazine as the starting material for alkylation or acid-catalyzed addition reactions.

 

The molecular structure of 2,4-Dichloro-6-(4-methoxyphenyl)-1,3,5-triazine and its derivatives has been a subject of study to understand their chemical behavior and properties. For example, the crystal structure of a related compound, 2-methoxy-4,6-bis(4-nitrophenoxy)-1,3,5-triazine, was determined using X-ray diffraction, revealing it belongs to the monoclinic system with detailed dimensional parameters, highlighting the structural complexity of these compounds .

 

Specification of CAS:90723-86-7 | 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine

 

ITEMS

SPECIFICATION

Melt point

132-133 °C

Boiling point

457.1±47.0 °C(Predicted)

Density

1.404±0.06 g/cm3(Predicted)

Form

Solid

Color

Creamy white

 

Research Application of CAS:90723-86-7 | 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine

 

Synthesis and UV Light Absorption : This compound has been synthesized through methods avoiding the Grignard reaction and used to create bis(resorcinyl) triazine derivatives as UV light absorbers (Jiang, Wang, & Li, 2008).

 

Photoinitiator in Polymerization : It serves as a radical reactive photoinitiator for UV-crosslinking of acrylic adhesives and acts as an effective co-initiator in photoinitiating systems under visible light (Kabatc, Czech, & Kowalczyk, 2011).

 

Dendrimer Synthesis : The compound has been used in the synthesis of 1,2,4-triazole dendrimers, providing a foundation for applications requiring a large number of heteroatoms or enhanced resistance to conditions (Maes, Verstappen, & Dehaen, 2006).

 

Synthesis of Functionalized Triazines : Research has focused on synthesizing sterically demanding triazines with functionalized groups for various applications (Werlé et al., 2017).

 

Applications in Antifungal Agents : Some derivatives of this compound have shown potential as antifungal agents (Sareen, Khatri, Jain, & Sharma, 2009).

 

Use in Polyamide Synthesis : This compound has been involved in the synthesis of thermally stable and organo-soluble polyamides, which are important in materials science (Hajibeygi, Faghihi, Khodaei-Tehrani, & Mirzakhanian, 2014).

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