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α-anisylbenzyl tert-butyl nitroxide is a complex organic compound that serves as a stable radical and is often used as a radical scavenger or inhibitor in various chemical reactions. It is characterized by a tert-butyl group attached to a nitroxide radical, which is in turn connected to an α-anisylbenzyl moiety. This structure endows the compound with unique properties, such as thermal stability and resistance to decomposition, making it a valuable tool in the field of radical chemistry. It is particularly useful in polymerization reactions, where it can control the molecular weight and structure of the resulting polymers by terminating radical chains. The compound's ability to quench radicals also makes it relevant in the study of free radical processes and in applications where the prevention of unwanted radical reactions is crucial.

63710-77-0

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63710-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63710-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,1 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63710-77:
(7*6)+(6*3)+(5*7)+(4*1)+(3*0)+(2*7)+(1*7)=120
120 % 10 = 0
So 63710-77-0 is a valid CAS Registry Number.

63710-77-0Downstream Products

63710-77-0Relevant academic research and scientific papers

Substituent Effects on ESR Parameters of α-Phenyl-N-tert-butylnitrone Spin Adducts. Resolution Enhancement and Mass Spectrometry

Pan, Kai,Lin, Chiou-Rong,Ho, Tong-Ing

, p. 632 - 638 (2007/10/02)

The combination of high-performance liquid chromatography (HPLC) and ESR spectrometry was used to isolate the free radicals produced by the reaction of a Grignard reagent with 15 substituted α-phenyl-N-tert-butylnitrones.Long-range hyperfine splitting con

Substituent Effect on the Spin-trapping Reactions of Substituted N-Benzylidene-t-butylamine N-oxides

Murofushi, Katsumi,Abe, Kazuhisa,Hirota, Minoru

, p. 1829 - 1834 (2007/10/02)

Relative rates of the reactions of substituted N-benzylidene-t-butylamine N-oxides with substituted phenyl free radicals have been determined by e.s.r. spectroscopic analyses of the products from competitive addition reactions.The substituent effect was interpreted in terms of a reaction mechanism involving an electron-transfer interaction between the reactants.The results are in accord with semiempirical MO calculations.

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