14453-65-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-aminophenyl)pyrrolidin-2-one is used as a performance-enhancing drug for its stimulant effects, which can temporarily increase alertness and focus. This makes it appealing for individuals seeking to improve cognitive performance in various settings, such as during exams or in high-pressure work environments.
Used in Weight Management:
Prolintane is used as an appetite suppressant, helping to control food intake and potentially leading to weight loss. Its ability to stimulate the central nervous system can reduce feelings of hunger, making it a candidate for weight management programs.
Used in Neurological Applications:
1-(2-aminophenyl)pyrrolidin-2-one is studied for its potential as a treatment for depression and cognitive impairment. Its influence on neurotransmitter levels, particularly norepinephrine and dopamine, suggests that it may have therapeutic benefits for individuals suffering from mood disorders or cognitive decline.
Used in Research:
In scientific research, Prolintane is utilized to study the effects of neurotransmitter reuptake inhibition on cognitive function and mood. This helps in understanding the underlying mechanisms of action for similar compounds and contributes to the development of new treatments for neurological conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 14453-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,5 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14453-65:
(7*1)+(6*4)+(5*4)+(4*5)+(3*3)+(2*6)+(1*5)=97
97 % 10 = 7
So 14453-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O/c11-8-4-1-2-5-9(8)12-7-3-6-10(12)13/h1-2,4-5H,3,6-7,11H2
14453-65-7Relevant academic research and scientific papers
Synthesis of annulated benzimidazoles via amidine cyclization
Liubchak, Kostiantyn,Nazarenko, Kostiantyn,Tolmachev, Andrey
scheme or table, p. 2993 - 3000 (2012/05/31)
Structurally diverse annulated benzimidazoles were synthesized via two copper(I)-catalyzed cyclocondensation reactions. In the first case the title compounds were prepared from lactams and o-bromoaniline. An alternative route consisted of an intramolecular cyclization of o-bromoarylamidines.
