phenoxy radical

Base Information

• Chemical Name: phenoxy radical
• CAS No.: 55748-05-5
• Molecular Formula: C₆H₅O
• Molecular Weight: 93.1051
• Mol file: 55748-05-5.mol

Synonyms:

Chemical Property of phenoxy radical

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of phenoxy radical

There total 63 articles about phenoxy radical which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 25.8%

2-phenoxy-1-phenylethanone (721-04-0) → phenyl benzyl ketone (451-40-1) + phenoxy radical (2122-46-5,55748-05-5) + 2-oxo-2-phenyl-ethyl (50781-28-7) + acetophenone (98-86-2) + phenacylacetophenone (495-71-6) + phenol (108-95-2,27073-41-2)

Guidance literature:

thiophenol; In benzene; Product distribution; Quantum yield; Kinetics; Irradiation;

DOI:10.1021/jo00288a019

Reference yield:

CH3I(1+)*CHCl3*Cl(1-) + phenol (108-95-2,27073-41-2) → chloroform (67-66-3,8013-54-5) + phenoxy radical (2122-46-5,55748-05-5) + methyl iodide (74-88-4)

Guidance literature:

In chloroform; at 22 ℃; Rate constant; multistep reaction;

DOI:10.1021/j100164a045

Reference yield:

cumyloxy radical (16812-36-5) + phenol (108-95-2,27073-41-2) → phenoxy radical (2122-46-5,55748-05-5) + 1-methyl-1-phenylethyl alcohol (617-94-7)

Guidance literature:

In tetrachloromethane; at 24.9 ℃; Rate constant; var. solvents; equilibrium constants for hydrogen bond formation between reagent and solvent;

DOI:10.1021/ja00115a029

upstream raw materials:

methoxybenzene

Phenetole

phenol

n-butyl phenyl ether

Downstream raw materials:

methoxybenzene

phenol

chlorine dioxide

phenolate