79289-23-9 Usage
Uses
Used in Medicinal Chemistry:
3-chloro-N-[(2,2-dimethyl-1-phenyl-propylidene)amino]propanamide is used as a potential antiviral agent in medicinal chemistry. It has been studied for its potential application in the treatment of hepatitis C virus, offering a promising therapeutic option for patients suffering from this viral infection.
Used in Pharmaceutical Drug Development:
3-chloro-N-[(2,2-dimethyl-1-phenyl-propylidene)amino]propanamide has also been investigated for its potential use in the development of new pharmaceutical drugs. Its unique structure and properties make it a valuable candidate for further research and development, with the potential to contribute to the creation of new therapeutic agents that can address various health conditions and diseases.
Used in Research and Development:
3-chloro-N-[(2,2-dimethyl-1-phenyl-propylidene)amino]propanamide plays a crucial role in research and development within the pharmaceutical industry. Its exploration and study can lead to advancements in drug discovery and the creation of innovative treatments for a wide range of medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 79289-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,8 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79289-23:
(7*7)+(6*9)+(5*2)+(4*8)+(3*9)+(2*2)+(1*3)=179
179 % 10 = 9
So 79289-23-9 is a valid CAS Registry Number.
79289-23-9Relevant academic research and scientific papers
Synthesis and properties of 3-oxo-1,2-diazetidinium ylides
Taylor, Edward C.,Haley, Neil F.,Clemens, Robert J.
, p. 7743 - 7752 (2007/12/18)
Treatment of α-chloroacylhydrazones of diaryl and certain aralkyl and dialkyl ketones with sodium hydride in anhydrous tetrahydrofuran gives 1-(disubstituted methylene)-3-oxo-1,2-diazetidinium inner salts (ylides). The reaction pathway involves formation of the hydrazone anion followed by intramolecular SN2 halide displacement (with complete inversion at the α carbon) by the sp2 imine nitrogen. These 1-(disubstituted methylene)-3-oxo-1,2-diazetidinium ylides are reduced by sodium borohydride to give 1-substituted 1,2-diazetidin-3-ones, undergo dipolar cycloaddition reactions to give fused aza-β-lactams, and can be hydrolyzed with p-toluenesulfonic acid monohydrate to the p-toluenesulfonic acid salt of 1,2-diazetidinone.
