56904-13-3 Usage
Uses
Used in Pharmaceutical Industry:
(1-benzyl-4-methylpiperazin-2-yl)methanamine is used as a potential therapeutic agent for the treatment of various conditions such as depression, anxiety, and neurological disorders. Its piperazine derivative structure and the presence of benzyl and methyl groups may contribute to its biological activity and pharmacological properties, making it a promising candidate for further research and development in the field of medicine.
Used in Research and Development:
(1-benzyl-4-methylpiperazin-2-yl)methanamine is used as a subject of research to explore its potential uses and effects in the field of medicine and pharmaceuticals. Further studies are needed to understand its mechanism of action, safety, and efficacy in treating specific conditions, as well as to optimize its formulation and delivery for therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 56904-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,0 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56904-13:
(7*5)+(6*6)+(5*9)+(4*0)+(3*4)+(2*1)+(1*3)=133
133 % 10 = 3
So 56904-13-3 is a valid CAS Registry Number.
56904-13-3Relevant academic research and scientific papers
Synthesis and structure-activity relationships of 4-amino-5-chloro-2- ethoxybenzamides with six- and seven-membered heteroalicycles as potential gastroprokinetic agents
Morie,Kato,Harada,Yoshida,Fujiwara,Matsumoto
, p. 1137 - 1147 (2007/10/02)
A new series of 4-amino-5-chloro-2-ethoxybenzamides 3b-f and 5-8 bearing six- and seven-membered heteroalicycles was prepared and evaluated for gastroprokinetic activity. Compounds 3b-e, derived by replacement of the morpholine oxygen of 4-amino-N-[(4-benzyl-2-morpholinyl)methyl]-5-chloro-2- ethoxybenzamide (3a) with other atoms (sulfur, nitrogen and carbon), generally exhibited a potent gastric emptying activity. N-(4-Benzyl-3- morpholinyl)methylbenzamide (5a) and its analogues 5b-e had weaker activity. However, N-(4-benzyl-3-morpholinyl)ethylbenzamide 8 was as potent as 3a. Benzamides 6a-e, having seven-membered heteroalicycles, showed fairly potent activity. Molecular superimpositions of 5a, 6a and 8 upon 3a using computer graphics suggested that the direction of the N-benzyl group greatly influences the gastric emptying activity, whereas the location of the alicyclic nitrogen is less critical.
