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CAS

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10384-15-3

2,4,6-Triphenylphenoxyl, also known as "triphenylphenoxy radical," is a stable free radical with the molecular formula C18H13O. It features a triphenylphenoxy group, which consists of three phenyl rings attached to a central phenoxy group. 2,4,6-Triphenylphenoxyl is commonly used as a model system for studying radical reactions, particularly in the field of polymer chemistry.

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  • 10384-15-3 Structure

  • Basic information

    1. Product Name: 2,4,6-Triphenylphenoxyl
    2. Synonyms: 2,4,6-Triphenylphenoxyl
    3. CAS NO:10384-15-3
    4. Molecular Formula: C48H34O2
    5. Molecular Weight: 321.39118
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10384-15-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4,6-Triphenylphenoxyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4,6-Triphenylphenoxyl(10384-15-3)
    11. EPA Substance Registry System: 2,4,6-Triphenylphenoxyl(10384-15-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10384-15-3(Hazardous Substances Data)

10384-15-3 Usage

Uses

Used in Polymer Chemistry Research:
2,4,6-Triphenylphenoxyl is used as a model compound for understanding the reactivity and behavior of organic radicals in polymer chemistry. It aids researchers in exploring the potential applications of radicals in radical polymerization and other organic chemistry reactions.
Used in Organic Chemistry Reactions:
2,4,6-Triphenylphenoxyl is employed as a stable free radical in various organic chemistry reactions. Its use helps in studying the mechanisms and kinetics of radical reactions, contributing to the advancement of organic chemistry knowledge and techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 10384-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,8 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10384-15:
(7*1)+(6*0)+(5*3)+(4*8)+(3*4)+(2*1)+(1*5)=73
73 % 10 = 3
So 10384-15-3 is a valid CAS Registry Number.

10384-15-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-triphenyl-4-(2,4,6-triphenyl-phenoxy)-cyclohexa-2,5-dienone

1.2 Other means of identification

Product number -
Other names 2,4,6-TRIPHENYLPHENOXYL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10384-15-3 SDS

10384-15-3Relevant articles and documents

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

Hayashi, Naoto,Ueno, Taisetsu,Okamoto, Naoki,Mori, Takahiro,Sasaki, Naho,Kamoto, Taku,Yoshino, Junro,Higuchi, Hiroyuki,Uekusa, Hidehiro,Tukada, Hideyuki

supporting information, p. 2547 - 2550 (2017/06/13)

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.

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