10384-15-3

Basic information

• Product Name: 2,4,6-Triphenylphenoxyl
• Synonyms: 2,4,6-Triphenylphenoxyl
• CAS NO: 10384-15-3
• Molecular Formula: C₄₈H₃₄O₂
• Molecular Weight: 321.39118
• Mol File: 10384-15-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4,6-Triphenylphenoxyl(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Triphenylphenoxyl(10384-15-3)
• EPA Substance Registry System: 2,4,6-Triphenylphenoxyl(10384-15-3)

Safety Data

• Hazardous Substances Data: 10384-15-3(Hazardous Substances Data)

Usage

General Description

2,4,6-Triphenylphenoxyl, also known as "triphenylphenoxy radical," is a chemical compound with the molecular formula C18H13O. It is a stable free radical and is commonly used as a model system for studying radical reactions, especially in the field of polymer chemistry. The compound has a triphenylphenoxy group, which consists of three phenyl rings attached to a central phenoxy group. 2,4,6-Triphenylphenoxyl is often used in research to understand the reactivity and behavior of organic radicals and to explore potential applications in radical polymerization and other organic chemistry reactions.

Upstream product

• 56-23-5 tetrachloromethane 
• 4647-83-0 2,4,6-triphenylphenoxyl radical 
• 67-66-3 chloroform 
• 3140-01-0 2,4,6-triphenylphenol 
• 75-05-8 acetonitrile 
• 71-43-2 benzene 
• 6864-20-6 2,4,6-triphenylaniline 
• 607-99-8 2,4,6-tribromoanisole 
• 98-80-6 phenylboronic acid 
• 115292-92-7 2,4,6-triphenylanisole 

Downstream Products

• 103404-41-7 2,4,6-tri-tert-butyl-4-(2,4,6-triphenyl-phenoxy)-cyclohexa-2,5-dienone 
• 103401-21-4 (2,4,6-triphenyl-phenyl)-trityl ether 
• 13505-55-0 4-Methoxy-2,4,6-triphenyl-cyclohexadien-(2,5)-on 
• 13505-56-1 4-Ethoxy-2,4,6-triphenyl-cyclohexadien-(2,5)-on 
• 3140-01-0 2,4,6-triphenylphenol 
• 13505-60-7 2-Acetoxy-2,4,6-triphenyl-cyclohexadien-(3,5)-on 
• 13505-59-4 2-Methoxy-2,4,6-triphenyl-cyclohexadien-(3,5)-on 

Relevant articles and documents

Binary amorphous solids consisting of 2,4,6-triarylphenoxyl radicals and their dimers

Although molecular amorphous materials represent an important area of research in solid-state chemistry, studies pertaining to these systems have been restricted almost exclusively to amorphous solids based on a single molecule. In this study, we found that, while the 2,4,6-bis(4-tert-butylphenyl)phenoxyl radical (2M) and its dimer (2D) did not give single-component amorphous solids, they rapidly formed the corresponding binary amorphous solid IIa following their condensation from benzene, dichloromethane, chloroform, and ethyl acetate solutions. The formation of IIa could be attributed to the good solubilities of 2M and 2D in these solvents and the high packing efficiencies of these amorphous solids. IIa was also obtained when crystals of 2D (IIb) were ground together. The solid-state formation of IIa would not only involve the locational exchange of 2M and 2D, but would also involve chemical exchanges.