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

Description

2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine is an organic compound that serves as an intermediate in the synthesis of Bemotrizinol (B131500), a broad-spectrum UV absorber capable of absorbing both UVA and UVB rays.

Uses

Used in Sunscreen Industry:
2,4-dichloro-6-(4-methoxyphenyl)-1,3,5-triazine is used as a chemical intermediate for the production of Bemotrizinol, a UV absorber that is incorporated into various sunscreens to protect the skin from harmful UV rays. Its ability to absorb both UVA and UVB rays makes it a valuable component in the formulation of effective sunscreen products.

Upstream product

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

Downstream Products

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

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

Manufacturing method of triazine-based compound and derivative thereof

The present invention relates to a triazine-based compound and a process for producing the same. The triazine compound according to an embodiment of the present invention may be prepared by reacting cyanuric acid (Cyanuric Chloride), anisole (anisole) and resorcinol (Resorcinol) to produce a triazine-based compound represented by Formula 1. Chemical Formula 1.

Polymerizable UV absorbers for the UV stabilization of polyesters. I. Design, synthesis and polymerization of a library of UV absorbing monomers

UV stabilizers, such as Tinuvin 1577, are organic additives that are used in the polymer industry to suppress polymer photodegradation, however leaching of the stabilizers from polymers is a significant practical issue which limits the effectiveness of the stabilizers and restricts polymer lifetimes. Novel, polymerizable UV stabilizers were synthesised and copolymerized with bis(2-hydroxyethyl) isophthalate to yield poly(ethylene isophthalate) copolymers where the UV stabilizers are bound covalently into the polymer chains. This strategy prevents leaching of stabilizers from polymers over time, and is expected to lead to enhanced UV protection of polymers compared to the admixing of polymers with UV stabilizers of low molar mass.