124668-47-9 Usage
Uses
Used in Pharmaceutical Industry:
3-Amino-3-methylazetidine dihydrochloride is used as a pharmaceutical ingredient for its potential role in the development of drugs targeting various medical conditions. Its unique structure and properties are under study to determine how it can be leveraged to improve drug efficacy and treatment options.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3-amino-3-methylazetidine dihydrochloride serves as a subject of research to explore its chemical properties and interactions with biological systems. This research is crucial for understanding how the compound can be modified or utilized in the creation of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 124668-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,6 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124668-47:
(8*1)+(7*2)+(6*4)+(5*6)+(4*6)+(3*8)+(2*4)+(1*7)=139
139 % 10 = 9
So 124668-47-9 is a valid CAS Registry Number.
124668-47-9Relevant academic research and scientific papers
Quantitative structure-activity relationships of antibacterial agents, 7-heterocyclic amine substituted 1-cyclopropyl-6,8-difluoro-4-oxoquinoline-3-carboxylic acids
Okada,Ezumi,Yamakawa,Sato,Tsuji,Tsushima,Motokawa,Komatsu
, p. 126 - 131 (2007/10/02)
Quantitative structure-activity relationships (QSAR) of various 7-(3-substituted-azetidin-1-yl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro -4-oxoquinoline-3-carboxylic acids, 14-25, were studied to clarify the structural requirements for 3-substituted azetidi
7-Azetidinylquinolones as antibacterial agents. Synthesis and structure- activity relationships
Frigola,Pares,Corbera,Vano,Merce,Torrens,Mas,Valenti
, p. 801 - 810 (2007/10/02)
A series of novel antibacterial quinolones and naphthyridones has been prepared which contain 7-azetidinyl substituents in place of the usual piperazine or aminopyrrolidine groups. These azetidinyl derivatives were evaluated for in vitro activity by deter
