205808-10-2 Usage
Uses
Used in Pharmaceutical Applications:
PPAP is used as a potential treatment for [application type] due to its stimulant and psychedelic properties. It has shown promise in animal studies for treating depression and other mood disorders, making it a candidate for further research and development in the pharmaceutical industry.
Used in Cognitive Enhancement:
PPAP is used as a cognitive enhancer for [application reason], as it has been studied for its potential to improve focus and attention. This application could be beneficial in various fields, such as education and professional settings, where enhanced cognitive function is desired.
Used in Addiction Treatment:
PPAP is used as a potential treatment for addiction and substance abuse for [application reason], given its stimulant properties and the need for alternative therapies to combat addiction. Further research is necessary to fully understand its effects and therapeutic potential in this area.
Used in Research and Development:
PPAP is used as a subject of research for [application reason], as it has shown potential in various applications, including mood disorder treatment, cognitive enhancement, and addiction treatment. Its unique properties make it an interesting compound for scientists and researchers to explore in the development of new therapies and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 205808-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,8,0 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 205808-10:
(8*2)+(7*0)+(6*5)+(5*8)+(4*0)+(3*8)+(2*1)+(1*0)=112
112 % 10 = 2
So 205808-10-2 is a valid CAS Registry Number.
205808-10-2Relevant academic research and scientific papers
Asymmetric synthesis of 3-substituted pyrrolidones via α-alkylation of a chiral non-racemic γ-lactam
Baussanne, Isabelle,Travers, Catherine,Royer, Jacques
, p. 797 - 804 (2007/10/03)
3-Alkyl pyrrolidones 9 were synthesized in good yield and high diastereoselectivity by α-alkylation of the new chiral non-racemic lactam 8 derived from (R)-(-)-phenylglycinol. After debenzylation and introduction of an electron-withdrawing group, 3-methylpyrrolidone 10 is easily hydrolyzed in a basic medium to produce γ-aminobutyric acid (GABA) analogue 13.
