73239-82-4 Usage
Uses
Used in Pharmaceutical Research:
[6-(4-methoxyphenyl)-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl](phenyl)methanone is used as a compound of interest in pharmaceutical research for its unique chemical structure and potential biological activities. [6-(4-methoxyphenyl)-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl](phenyl)methanone's specific application reason is its potential to contribute to the development of new drugs or therapies, given its distinctive molecular composition.
Used in Chemical Synthesis:
In the chemical industry, [6-(4-methoxyphenyl)-2-phenyl-5,6-dihydro-4H-1,3,4-oxadiazin-4-yl](phenyl)methanone may be used as a synthetic intermediate for the creation of more complex molecules or pharmaceutical agents. Its application reason lies in its structural diversity and the possibility of further functionalization to achieve desired biological effects.
Check Digit Verification of cas no
The CAS Registry Mumber 73239-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73239-82:
(7*7)+(6*3)+(5*2)+(4*3)+(3*9)+(2*8)+(1*2)=134
134 % 10 = 4
So 73239-82-4 is a valid CAS Registry Number.
73239-82-4Relevant academic research and scientific papers
Reactions of dibenzoyldiazene. Part 1. Cycloaddition and the inhibition and retardation of vinyl addition polymerizations
Bassam, Farideh,Jones, Richard G.
, p. 1759 - 1766 (2007/10/02)
The cycloaddition of dibenzoyldiazine to a selection of monomers with electron-rich vinyl groups has been shown to compette with its capability as an inhibitor of their polymerization by a free-radical mechanism.Cycloaddition to monomers with electron-deficient vinyl groups does not occur, and dibenzoyldiazene acts solely as a retarder of their polymerization.Kinetic mechanisms compatible with the experimental observations are proposed.
