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α-(p-Nitrophenyl)-N-(2,6-dimethylphenyl)nitrone is a complex organic compound with the chemical formula C17H14N4O4. It is a derivative of nitrone, a class of compounds known for their ability to trap free radicals, making them useful in various applications such as antioxidants, spin traps in electron spin resonance spectroscopy, and in the study of radical reactions. This particular compound features a nitrone functional group attached to a p-nitrophenyl group and a 2,6-dimethylphenyl group, which contributes to its chemical reactivity and stability. Due to its structural characteristics, it is often employed in the field of chemistry for research purposes, particularly in the investigation of radical reactions and as a potential antioxidant.

72725-83-8

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72725-83-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72725-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,2 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72725-83:
(7*7)+(6*2)+(5*7)+(4*2)+(3*5)+(2*8)+(1*3)=138
138 % 10 = 8
So 72725-83-8 is a valid CAS Registry Number.

72725-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name α-(p-Nitrophenyl)-N-(2,6-dimethylphenyl)nitrone

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:72725-83-8 SDS

72725-83-8Relevant academic research and scientific papers

Synthesis and Reactions of Derivatives of 6-Imino-2,4-cyclohexadien-1-ols

Stahl, Mark A.,Kenesky, Bernadine F.,Berbee, Robertus P. M.,Richards, Matthew,Heine, Harold W.

, p. 1197 - 1202 (1980)

α-(p-Nitrophenyl)-N-(2,6-dimethylphenyl)nitrone (6a) and α-(p-nitrophenyl)-N-(2,4,6-trimethylphenyl)nitrone (6b) are isomerized by p-nitrobenzoyl chloride in anhydrous ether into N-(2,6-dimethylphenyl)-p-nitrobenzamide (7a) and N-(2,4,6-trimethylphenyl)-p

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