117186-74-0 Usage
Uses
Used in Pharmaceutical Development:
(S)-N-(2-Benzoylphenyl)-2-pyrrolidinecarboxamide is used as a potential therapeutic agent for the development of pharmaceutical drugs. Its unique structure and chirality may contribute to its efficacy in treating various conditions.
Used in Neurological Disorders Treatment:
In the field of medicinal chemistry, (S)-N-(2-Benzoylphenyl)-2-pyrrolidinecarboxamide is considered for its potential role in managing neurological disorders. Its specific spatial arrangement could be key to targeting and treating these conditions effectively.
Used in Pain Management:
(S)-N-(2-Benzoylphenyl)-2-pyrrolidinecarboxamide is also being explored for its use in pain management, where its unique properties may offer new avenues for the development of analgesics.
Used as a Potential Antiviral Agent:
(S)-N-(2-Benzoylphenyl)-2-pyrrolidinecarboxamide is under investigation for its potential as an antiviral agent, suggesting that it could be utilized in the development of treatments for viral infections.
Further research and testing are necessary to fully understand the compound's potential uses and effects, ensuring its safety and efficacy in various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 117186-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,8 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 117186-74:
(8*1)+(7*1)+(6*7)+(5*1)+(4*8)+(3*6)+(2*7)+(1*4)=130
130 % 10 = 0
So 117186-74-0 is a valid CAS Registry Number.
117186-74-0Relevant academic research and scientific papers
Synthesis of 5-arylpyrrolo[2,1-c][1,4]benzodiazepines under mild cyclodehydration conditions
Legerén, Loreto,Domínguez, Domingo
experimental part, p. 2718 - 2722 (2010/05/02)
The efficiency of a cyclodehydration reaction leading to benzodiazepinones is markedly improved by N-methylation of the amide link connecting the nucleophile and the electrophile, which is attributed to its favouring both the more reactive E-rotamer and the exit of the leaving group.
Enantiospecific synthesis of 5-phenylpyrrolo[2,1-c][1,4]benzodiazepines
Legerén, Loreto,Gómez, Eduardo,Domínguez, Domingo
scheme or table, p. 7174 - 7177 (2009/04/10)
Enantiomerically pure 5-phenylpyrrolo[2,1-c][1,4]benzodiazepines were synthesized starting from 2-aminobenzophenones and 2-amino-4-methoxyxanthone, using l-proline as a chiral building block.
