3174-49-0 Usage
Description
(2-methylphenyl)oxidanyl, also known as the 2-methylphenyl radical, is a highly reactive organic compound with the chemical formula C7H7O. It is a type of free radical, meaning it has an unpaired electron and is therefore very unstable and reactive.
Used in Organic Synthesis:
(2-methylphenyl)oxidanyl is used as an intermediate in organic synthesis for its reactivity, which makes it useful for various types of chemical reactions.
Used in Pharmaceutical Production:
(2-methylphenyl)oxidanyl is used as a reactant in the production of pharmaceuticals, due to its unique properties and reactivity.
Used in Agrochemical Production:
(2-methylphenyl)oxidanyl is used as a reactant in the production of agrochemicals, taking advantage of its reactivity in chemical reactions.
Used in Specialty Chemicals Production:
(2-methylphenyl)oxidanyl is used as a reactant in the production of specialty chemicals, owing to its unique properties and reactivity.
Used in Radical Chemistry Research:
(2-methylphenyl)oxidanyl is used as a subject of study in radical chemistry and reactions, due to its instability and reactivity.
Note: Due to its instability and reactivity, strict handling and safety protocols are necessary when working with (2-methylphenyl)oxidanyl.
Check Digit Verification of cas no
The CAS Registry Mumber 3174-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3174-49:
(6*3)+(5*1)+(4*7)+(3*4)+(2*4)+(1*9)=80
80 % 10 = 0
So 3174-49-0 is a valid CAS Registry Number.
3174-49-0Relevant articles and documents
Kinetics and mechanisms of reactions of the nitrate radical (NO 3) with substituted phenols in aqueous solution
Barzaghi, Paolo,Herrmann, Hartmut
, p. 5379 - 5388 (2004)
Second order rate constants were obtained for the reactions of the nitrate radical (NO3) with substituted phenols in aqueous solutions at 298 K and pH = 0.5. The following compounds were investigated and the corresponding rate constants are rep
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
