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(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.

3174-49-0

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3174-49-0 Usage

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.

3174-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-λ<sup>1</sup>-oxidanyl-2-methylbenzene

1.2 Other means of identification

Product number -
Other names 2-Methyl-phenoxy-radikal

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:3174-49-0 SDS

3174-49-0Upstream product

3174-49-0Downstream Products

3174-49-0Relevant academic research and scientific papers

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

Reaction of tert-Butoxy Radicals with Phenols. Comparison with the Reactions of Carbonyl Triplets

Das, P. K.,Encinas, M. V.,Steenken, S.,Scaiano, J. C.

, p. 4162 - 4166 (2007/10/02)

Tert-butoxy radicals generated in the photodecomposition of di-tert-butyl peroxide react efficiently with phenols to yield the corresponding phenoxy radicals.Typical rate constants in benzene at 22 deg C are 3.3x108 and 1.6x109 Msup

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