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The 2-Naphthylmethyl radical, also known as 2-(2-naphthoyl)propane-1-yl, is an organic compound with the chemical formula C13H13. It is a radical species derived from 2-naphthoic acid, where the carboxylic acid group is replaced by a methyl group. This radical is characterized by its aromatic structure, with a naphthalene ring attached to a three-carbon chain. It is often used in the synthesis of various organic compounds, particularly those with potential applications in pharmaceuticals and materials science. The 2-Naphthylmethyl radical is known for its stability and reactivity, which can be further modified through various chemical reactions.

7419-61-6

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7419-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7419-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7419-61:
(6*7)+(5*4)+(4*1)+(3*9)+(2*6)+(1*1)=106
106 % 10 = 6
So 7419-61-6 is a valid CAS Registry Number.

7419-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methylnaphthalene radical

1.2 Other means of identification

Product number -
Other names 2-naphtho-methyl radical

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:7419-61-6 SDS

7419-61-6Downstream Products

7419-61-6Relevant academic research and scientific papers

Mesolysis Mechanisms of Aromatic Thioether Radical Anions Studied by Pulse Radiolysis and DFT Calculations

Yamaji, Minoru,Tojo, Sachiko,Fujitsuka, Mamoru,Sugimoto, Akira,Majima, Tetsuro

, p. 7890 - 7895 (2015/09/01)

The mesolysis mechanisms for eight aromatic thioether radical anions (ArCH2SAr′?-) generated during radiolysis in 2-methyltetrahydrofuran were studied by spectroscopic measurements and DFT calculation. Seven of ArCH2SAr′s

CLEVEAGE RATES FOR RADIOLYSIS-PRODUCED RADICAL ANIONS OF NAPHTHYLMETHYL PHENYL ETHERS AND NAPHTHYL BENZYL ETHERS

Guthrie, Robert D.,Patwardhan, Manjiri,Chateauneuf, John E.

, p. 147 - 152 (2007/10/02)

Cleveage reactions of α- and β-naphthylmethyl phenyl ethers and of α- and β-naphthyl benzyl ethers were studied by pulse radiolysis.Transient spectra indicate that reactions occur via electron capture followed by cleavage of the resultant radical anions to give arylmethyl radicals and aryloxide ions.Product studies of extensively irradiated samples are consistent with this scheme and show patterns which are informative for radiation studies in general.The reactions were studied in several solvents.The behavior of transient spectra obtained in acetonitrile for these ethers shows clearly that radical anions of the naphthylmethyl ethers cleave more rapidly than do the radical anions of the naphthyl benzyl ethers.

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