90723-86-7

Basic information

• Product Name: 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine
• Synonyms: 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine;1,3,5-Triazine,2,4-dichloro-6-(4-methoxyphenyl;2,4-dichloro-6-(4-methoxyphenyl)-
• CAS NO: 90723-86-7
• Molecular Formula: C₁₀H₇Cl₂N₃O
• Molecular Weight: 256.08808
• EINECS: 604-604-1
• Mol File: 90723-86-7.mol
• Article Data: 22

Chemical Properties

• Melting Point: 132-133 °C
• Boiling Point: 457.1±47.0 °C(Predicted)
• Appearance: /
• Density: 1.404±0.06 g/cm3(Predicted)
• Solubility: Benzene, DCM, Ethyl Acetate,
• PKA: -1.37±0.10(Predicted)
• CAS DataBase Reference: 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine(90723-86-7)
• EPA Substance Registry System: 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine(90723-86-7)

Safety Data

• Hazardous Substances Data: 90723-86-7(Hazardous Substances Data)

Usage

Uses

2,4-Dichloro-6-(4-methoxyphenyl)-1,3,5-triazine is an intermediate in the synthesis of Bemotrizinol (B131500) broad-spectrum UV absorber, absorbing both UVA and UVB. Bemotrizinol is added to various sunscreens to absorb UV rays.

Upstream product

• 100-07-2 4-methoxy-benzoyl chloride 
• 127099-85-8 N-Cyanoguanidine 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 108-78-1 2,4,6-triamino-s-triazine 
• 5720-07-0 4-methoxyphenylboronic acid 
• 73774-45-5 di-(4-methoxyphenyl)borinic acid 
• 100-66-3 methoxybenzene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 187393-00-6 tinosorb S 
• 1440-00-2 4-[4-(2,4-dihydroxyphenyl)-6-(4-methoxyphenyl)-1,3,5-triazin-2-yl]benzene-1,3-diol 
• 1147997-11-2 2,4-bis(4-trimethylsilylmethoxycarbonylphenylamino)-6-(para-methoxyphenyl)-s-triazine 
• 1147997-12-3 2,4-bis(3-hydroxy-4-trimethylsilylmethoxycarbonylphenylamino)-6-(para-methoxyphenyl)-s-triazine 
• 21902-35-2 2-chloro-4,6-bis(4-methoxyphenyl)-1,3,5-triazine 
• 67014-53-3 4-(4,6-bis(4-methoxyphenyl)-1,3,5-triazin-2-yl)benzaldehyde 

Relevant articles and documents

Synthesis, characterization, and antimicrobial screening of s-triazines linked with piperazine or aniline scaffolds

Two series of s-triazines linked with piperazine or aniline scaffolds (4a-i and 5a-j) were synthesized and evaluated for their in vitro biological efficacy against Gram positive and Gram negative bacteria (Klebsiella pneumoniae MTCC 109, Pseudomonas aerug

Preparation method of 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine

The invention discloses a preparation method of 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine. According to the preparation method, p-methoxyphenylboronic acid and cyanuric chloride are taken as raw materials and a magnetic silicon dioxide supported palladium complex is taken as a catalyst, an alkali and a solvent are added, Suzuki coupling reaction is conducted, a catalyst phase is separated out after the reaction, the solvent is recovered from a product phase, and finally, recrystallizing and drying are conducted to obtain a pure product 2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine. The catalyst can be separated, recovered and recycled through an external magnetic field, the magnetic catalyst is high in activity, high in catalytic efficiency and high in reaction selectivity, the product purity is high, operation is simple, reaction conditions are mild, the reaciton process is clean and friendly, and the method provided by the invention is a novel green and efficient preparation method.

TRIAZINE UV ABSORBERS AND A PROCESS FOR THE PREPARATION THEREOF

The presently claimed invention relates to novel, highly efficient triazine UV absorbers and a general process for the preparation UV absorber compounds from natural precursors.