4166-09-0 Usage
Description
1-Phenyl-2-thioxopyrrolidin-5-one, commonly known as Prolintane, is a synthetic stimulant with the molecular formula C10H9NOS. It is a derivative of pyrrolidine and has been recognized for its central nervous system stimulant properties. Initially developed as a potential treatment for depression and fatigue, Prolintane has also been reported to possess nootropic effects, enhancing cognitive function and memory. Despite its potential therapeutic uses, the compound's mechanism of action remains not fully understood, but it is believed to increase the levels of dopamine and norepinephrine in the brain. Due to its potential for abuse and dependence, the use and sale of Prolintane are now restricted in many countries.
Uses
Used in Pharmaceutical Industry:
1-Phenyl-2-thioxopyrrolidin-5-one is used as a central nervous system stimulant for its potential therapeutic effects in treating conditions such as depression and fatigue. Its ability to increase the levels of dopamine and norepinephrine in the brain contributes to its stimulant properties, which may help alleviate symptoms of these conditions.
Used in Cognitive Enhancement:
1-Phenyl-2-thioxopyrrolidin-5-one is used as a nootropic agent to improve cognitive function and memory. Its nootropic effects may be beneficial for individuals seeking to enhance their cognitive performance or for those experiencing memory-related issues.
However, it is important to note that due to the potential for abuse and dependence, the use of 1-Phenyl-2-thioxopyrrolidin-5-one in these applications is subject to regulatory restrictions in many countries.
Check Digit Verification of cas no
The CAS Registry Mumber 4166-09-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4166-09:
(6*4)+(5*1)+(4*6)+(3*6)+(2*0)+(1*9)=80
80 % 10 = 0
So 4166-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NOS/c12-9-6-7-10(13)11(9)8-4-2-1-3-5-8/h1-5H,6-7H2
4166-09-0Relevant articles and documents
Synthesis of lactams by regioselective reduction of cyclic dicarboximides
Milewska, Maria J.,Bytner, Tomasz,Polonski, Tadeusz
, p. 1485 - 1488 (2007/10/03)
Lactams can be obtained by the monothionation of imides with Lawesson's reagent followed by the desulfurization of resulted monothioimides with Raney nickel.
