69540-76-7 Usage
Chemical class
2-(methylsulfanyl)-4-(pyrrolidin-1-yl)-3H-1,5-benzodiazepine belongs to the benzodiazepine class of drugs, which are known for their sedative, anxiolytic, and muscle relaxant properties.
Psychoactive potential
2-(methylsulfanyl)-4-(pyrrolidin-1-yl)-3H-1,5-benzodiazepine has potential psychoactive properties, meaning it may affect the user's mental state, emotions, or behavior.
Methylsulfanyl group
The presence of a methylsulfanyl group in the molecule may contribute to its impact on the central nervous system, potentially enhancing its sedative or anxiolytic effects.
Pyrrolidin-1-yl group
The pyrrolidin-1-yl group is another structural feature that may influence the compound's effects on the central nervous system, possibly contributing to its potential pharmacological activity.
3H-1,5-benzodiazepine backbone
The 3H-1,5-benzodiazepine backbone is a characteristic structure found in many drugs with sedative or hypnotic effects, suggesting that 2-(methylsulfanyl)-4-(pyrrolidin-1-yl)-3H-1,5-benzodiazepine may share similar properties.
Potential pharmacological activity
Due to its structural features and belonging to the benzodiazepine class, 2-(methylsulfanyl)-4-(pyrrolidin-1-yl)-3H-1,5-benzodiazepine may have potential pharmacological activity, making it a candidate for further research and development.
Therapeutic applications
If proven effective and safe, 2-(methylsulfanyl)-4-(pyrrolidin-1-yl)-3H-1,5-benzodiazepine could potentially be used as a sedative, anxiolytic, or muscle relaxant for the treatment of various conditions related to anxiety, insomnia, or muscle tension.
Check Digit Verification of cas no
The CAS Registry Mumber 69540-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,4 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69540-76:
(7*6)+(6*9)+(5*5)+(4*4)+(3*0)+(2*7)+(1*6)=157
157 % 10 = 7
So 69540-76-7 is a valid CAS Registry Number.
69540-76-7Relevant academic research and scientific papers
Research on 1,5-benzodiazepines. III.
Roma,Vigevani,Balbi,Ermili
, p. 62 - 71 (2007/10/09)
Treatment of 2,3-dihydro-2-oxo-4-dialkylamino-1H-1,5-benzodiazepines with phosphorus pentasulfide afforded 2-thio derivatives which in turn gave the corresponding methylmercapto derivatives by reaction with sodium hydride and methyl iodide. By treating these compounds with dialkylamines the formation of 2,4-bisdialkylamino-3H-1,5-benzodiazepines was achieved. Pharmacological screening of some of the products indicated that the introduction of a second dialkylamino substituent into the 1,5-benzodiazepine molecule gave the compounds CNS excitant properties, while the initial monodialkylamino derivatives containing sulfur showed a CNS depressant activity.
