23449-07-2

Basic information

• Product Name: 2-(4-methoxyphenyl)-4,6-diphenyl-1,3,5-triazine
• Synonyms: 2-(4-methoxyphenyl)-4,6-diphenyl-1,3,5-triazine
• CAS NO: 23449-07-2
• Molecular Formula: C₂₂H₁₇N₃O
• Molecular Weight: 339.38988
• Mol File: 23449-07-2.mol
• Article Data: 15

Chemical Properties

• Melting Point: 157.5-158.5 °C
• Boiling Point: 568.8±52.0 °C(Predicted)
• Appearance: /
• Density: 1.174±0.06 g/cm3(Predicted)
• PKA: 1.17±0.10(Predicted)
• CAS DataBase Reference: 2-(4-methoxyphenyl)-4,6-diphenyl-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxyphenyl)-4,6-diphenyl-1,3,5-triazine(23449-07-2)
• EPA Substance Registry System: 2-(4-methoxyphenyl)-4,6-diphenyl-1,3,5-triazine(23449-07-2)

Safety Data

• Hazardous Substances Data: 23449-07-2(Hazardous Substances Data)

Usage

Type of compound

Organic compound

Primary use

UV filter in sunscreens and other cosmetic products

Protection range

Both UVA and UVB rays

Mechanism of action

Absorbs and dissipates UV radiation to prevent skin damage

Chemical structure

Triazine ring and phenyl groups

Key properties

Photostability, safety, and strong UV-absorbing capabilities

Environmental concerns

Potential impact on aquatic ecosystems and bioaccumulation

Ongoing research

Regulations and usage due to environmental concerns

Upstream product

• 3842-55-5 2-chloro-4,6-diphenyl-1,3,5-triazine 
• 5720-07-0 4-methoxyphenylboronic acid 
• 116856-96-3 2,5-Bis-(4-nitro-phenyl)-4,6-diphenyl-2,5-dihydro-[1,2,3,5]tetrazine 
• 116856-91-8 1,2-bis(p-nitrophenylazo)stilbene 
• 22265-37-8 4-methoxybenzamidine 
• 134-81-6 benzil 
• 104-01-8 4-Methoxyphenylacetic acid 
• 1670-14-0 benzamidine monohydrochloride 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 2393-23-9 4-methoxy-benzylamine 
• 702-24-9 4-methoxy-N-methylbenzylamine 
• 104-93-8 p-methylanizole 
• 100-47-0 benzonitrile 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 7753-02-8 4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenol 

Relevant articles and documents

NOVEL COMPOUND FOR ORGANIC LIGHT-EMITTING DIODE AND COATING COMPOSITION FOR ORGANIC LAYER COMPRISING THE SAME

The present invention relates to a compound represented by general formula ((1) I), and a (1) coating solution composition comprising the same as. described in the detailed description of the present invention, as described in the detailed description of

Transition Metal-Free sp3 C–H Functionalization of Arylacetic Acids for the Synthesis of 1,3,5-Triazines

A one-pot simple, efficient and practically viable protocol for the synthesis of substituted 1,3,5-triazines has been reported from arylacetic acids and benzamidine hydrochloride. In addition, we demonstrated first transition metal-free conversion of phenylacetic acid to benzaldehyde which on condensation with two equivalents of benzamidine hydrochloride offered 2,4,6-trisubstituted 1,3,5-triazines. This protocol is environmentally benign and economically viable which makes it feasible for gram scale synthesis.

A 1, 3, 5 - triazine derivative synthesis method

The invention relates to a synthesis method of 1,3,5-triazine derivatives. The synthesis method comprises the steps of mixing amidine hydrochloride, alcohol, hydrated copper acetate and sodium carbonate, adding a solvent, reacting for 12 hours-24 hours in air at the temperature of 110 DEG C-120 DEG C to obtain a product, purifying the product, extracting, drying, concentrating and separating by virtue of column chromatography to obtain the 1,3,5-triazine derivatives. The synthesis method of the 1,3,5-triazine derivatives, which is disclosed by the invention has the advantages of low cost, available raw materials, high synthesis efficiency and wide application range and is suitable for reaction of a plurality of substrates.