41115-75-7 Usage
Description
(3-methylphenyl)oxidanyl, also known as 3-methoxyphenyloxyl or 3-methylphenylperoxy, is a chemical compound with the molecular formula C7H7O. It is a radical species, meaning it contains an unpaired electron, making it highly reactive. This reactivity allows it to participate in various chemical reactions, including radical chain processes.
Uses
Used in Organic Synthesis:
(3-methylphenyl)oxidanyl is used as a reactive intermediate in organic synthesis for its ability to participate in various chemical reactions, including radical chain processes.
Used in Polymerization Reactions:
In the polymer industry, (3-methylphenyl)oxidanyl is used as a catalyst or initiator to promote polymerization reactions, taking advantage of its radical nature to initiate the process.
Used in Pharmaceutical Production:
(3-methylphenyl)oxidanyl serves as a key intermediate in the production of various pharmaceuticals, contributing to the synthesis of drug molecules that require its specific reactive properties.
Used in Agrochemical Production:
Similarly, in the agrochemical industry, (3-methylphenyl)oxidanyl is utilized as an intermediate in the synthesis of various agrochemical products, such as pesticides and herbicides, due to its reactivity and role in chemical reactions.
It is important to handle (3-methylphenyl)oxidanyl with care due to its reactivity and potential hazards, making safety a priority in its application across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 41115-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41115-75:
(7*4)+(6*1)+(5*1)+(4*1)+(3*5)+(2*7)+(1*5)=77
77 % 10 = 7
So 41115-75-7 is a valid CAS Registry Number.
41115-75-7Relevant articles and documents
A laser flash photolysis and theoretical study of hydrogen abstraction from phenols by triplet α-naphthoflavone
De Lucas, Nanci C.,Fraga, Helena S.,Cardoso, Cristiane P.,Correa, Rodrigo J.,Garden, Simon J.,Netto-Ferreira
experimental part, p. 10746 - 10753 (2011/05/19)
The hydrogen abstraction (HA) reaction by the triplet of α-naphthoflavone (1) has been investigated experimentally by the use of laser flash photolysis (LFP) and theoretically with density functional theory (DFT) and atoms in molecules (AIM). The triplet
Photophysical Properties of Methylated Phenols in Nonpolar Solvents
Grabner, G.,Koehler, G.,Marconi, G.,Monti, S.,Venuti, E.
, p. 3609 - 3613 (2007/10/02)
The photophysical properties of phenol and a series of mono-, di-, and trimethyl-substituted phenols excited in their first singlet state in hydrocarbon solvents have been investigated by measuring fluorescence lifetimes and quantum yields and lowest trip
Substituent Effects on Rates of One-Electron Oxidation of Phenols by the Radicals ClO2, NO2, and SO3(1-)
Alfassi, Zeev B.,Huie, Robert E.,Neta, P.
, p. 4156 - 4158 (2007/10/02)
Rate constants for the reactions of ClO2, NO2, and SO3(1-) radicals with several substituted phenoxide ions have been measured by pulse radiolysis.They vary from the immeasurably slow (4) to almost diffusion-controlled rates (>109 M-1 s-1) and depend on the redox potentials of the phenoxide ions and the inorganic radicals.With the weak oxidant SO3(1-) reverse reactions were observed in certain cases; i.e., the phenoxyl radical oxidizes sulfite ions.An attempt is made to correlate the rate constants with Hammett's substituent constants and the results are compared with those obtained previously for the reactions of various inorganic radicals with phenols and phenoxide ions.
