331947-63-8 Usage
Description
(R)-7-chloro-5-methoxymethyloxy-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepine is a complex benzazepine compound characterized by the presence of chloro, methoxy, and benzoylamino groups. Structurally, it resembles the antipsychotic drug aripiprazole, suggesting potential pharmaceutical applications, particularly in the treatment of psychiatric disorders. Further research and testing are necessary to determine its specific pharmacological properties and therapeutic uses.
Uses
Used in Pharmaceutical Industry:
(R)-7-chloro-5-methoxymethyloxy-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepine is used as a potential therapeutic agent for psychiatric disorders due to its structural similarity to the antipsychotic drug aripiprazole. Its application aims to explore its potential in treating various mental health conditions, pending further research and clinical trials.
Used in Research and Development:
In the field of medicinal chemistry, this compound serves as a valuable research tool for understanding the structure-activity relationships of benzazepine derivatives. It can be used to investigate the effects of different functional groups on the pharmacological properties of benzazepines, potentially leading to the development of new and improved antipsychotic medications.
Check Digit Verification of cas no
The CAS Registry Mumber 331947-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,9,4 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 331947-63:
(8*3)+(7*3)+(6*1)+(5*9)+(4*4)+(3*7)+(2*6)+(1*3)=148
148 % 10 = 8
So 331947-63-8 is a valid CAS Registry Number.
331947-63-8Relevant articles and documents
An efficient synthesis of optical isomers of vasopressin V2 receptor antagonist OPC-41061 by lipase-catalyzed enantioselective transesterification
Matsubara, Jun,Morita, Seiji,Yamashita, Hiroshi,Otsubo, Kenji,Kitano, Kazuyoshi,Ohtani, Tadaaki,Kawano, Yoshikazu,Bando, Masahiko,Kido, Masaru,Ochida, Minoru,Tabusa, Fujio
, p. 131 - 138 (2007/10/03)
The optically active enantiomers of 7-chloro-5-hydroxy-1-[2- methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro- 1H- 1-benzazepine (OPC-41061, 1) were enantioselectively synthesized. The chiral acetate ((R)-(-)-3) and the chiral alcohol ((S)-(+)-2) were prepared via the resolution of the racemic alcohol ((±)-2) using the lipase-mediated transesterification with vinyl acetate. Compounds ((R)-(-)-3) and ((S)-(+)-2) were converted to optically active 1.
