65647-22-5 Usage
Chemical class
Quaternary ammonium salt
A compound with a central nitrogen atom bonded to four alkyl or aryl groups.
Common use
Pharmaceutical research
Frequently utilized to study the effects of drugs and their potential therapeutic applications.
Piperidine ring
A six-membered heterocyclic ring with one nitrogen atom.
Piperidinium cation
A positively charged ion derived from the piperidine ring.
Iodide anion
A negatively charged ion with one iodine atom and a single negative charge.
Benzodiazepine structure
A heterocyclic aromatic ring system consisting of two fused benzene rings and a seven-membered nitrogen-containing ring.
Phenyl group
A carbon-based ring structure with six carbon atoms and a single hydrogen atom attached to the benzodiazepine structure.
Derivative of benzodiazepine
1-methyl-1-[2-(5-oxo-1-phenyl-1,2,3,5-tetrahydro-4H-1,4-benzodiazepin-4-yl)ethyl]piperidinium iodide is a modified version of the benzodiazepine structure.
Functionality
Studying benzodiazepine receptors in the brain
The compound is used to investigate the role of benzodiazepine receptors in the brain and their potential therapeutic applications.
Neuroscience
The compound may have applications in the field of neuroscience, contributing to the understanding of brain functions and related disorders.
Lead compound for new medications
1-methyl-1-[2-(5-oxo-1-phenyl-1,2,3,5-tetrahydro-4H-1,4-benzodiazepin-4-yl)ethyl]piperidinium iodide may serve as a starting point for the development of new drugs targeting neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 65647-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65647-22:
(7*6)+(6*5)+(5*6)+(4*4)+(3*7)+(2*2)+(1*2)=145
145 % 10 = 5
So 65647-22-5 is a valid CAS Registry Number.
65647-22-5Relevant academic research and scientific papers
Synthesis and pharmacological activity and some derivatives of1-phenyl-1,2,3,4-tetrahydro-5H-1,4-benzodiazepin-5-one
Bagolini,De Witt,Pacifici,Ramacci
, p. 476 - 480 (2007/10/09)
4-N-Alkylamino derivatives and corresponding ammonium quaternary salts of tetrahydro-l,4-benzodiazepin-5-one were synthesized and evaluated for psychotropic activity in mice by ip via. This study was also extended to some nitro and amino derivatives of tetrahydro-1,4-benzodiazepin-5-one. Compounds were devoid of tranquilizing activity and in comparison with two classical benzodiazepines, chlordiazepoxide and diazepam, they showed high toxicity and little or no effect on motor coordination, motor activity, and maximal electroshock. On some 'in vitro' tests the compounds exhibited pharmacological properties when they were used at high concentrations.
