60390-52-5 Usage
Chemical structure
The compound consists of a 1-butanone group, a 4-fluorophenyl group, and an octahydropyrazino[1,2-a]azepin-2(1H)-yl group linked together.
Synthetic chemical
It is a synthetically produced chemical, which means it is not found naturally and is created through chemical reactions.
Potential applications
The compound has potential pharmaceutical and industrial applications, although the specific uses may vary depending on its formulation and context.
Interaction with biological systems
The compound may have the ability to interact with biological systems, which could be relevant for its pharmaceutical applications.
Building block for other compounds
It can potentially serve as a building block or intermediate for the synthesis of other compounds, contributing to its industrial applications.
Variability in properties and uses
The specific properties and uses of this chemical may vary depending on its formulation and how it is used in different contexts, highlighting the importance of understanding its behavior in various situations.
Check Digit Verification of cas no
The CAS Registry Mumber 60390-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,9 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60390-52:
(7*6)+(6*0)+(5*3)+(4*9)+(3*0)+(2*5)+(1*2)=105
105 % 10 = 5
So 60390-52-5 is a valid CAS Registry Number.
60390-52-5Relevant academic research and scientific papers
Studies in Potential Filaricides: Part XIII - Synthesis of 1,4-Diazabicyclononanes, 1,4-Diazabicyclodecanes and 1,4-Diazabicycloundecanes as diethylcarbamazine Analogs
Shukla, U. K.,Khanna, J. M.,Sharma, Satyavan,Anand, Nitya,Chatterjee, R. K.,Sen, A. B.
, p. 664 - 668 (2007/10/02)
1,4-Diazabicyclononanes (13 - 20), 1,4-diazabicyclodecanes (21 - 28), 1,4-diazabicycloundecanes (29 - 34), 1,4-diazabicyclononan-5-ones (37 - 41) and 1,4-diazabicyclodecan-5-ones (42 - 44) having alkyl and acyl substituents at 4-position have been synthesized and evaluated for their filaricidal activity against Litomasoides carinii infection in cotton rats.Except 4-diethylcarbamoyl-1,4-diazabicyclononane (13), which exhibits significant activity, being about 3/5th as active as the standard diethylcarbamazine (DEC), none of the other compounds shows any activity against adult worms.The results have been rationalised in terms of critical bulk around the N-1 of the piperazine ring of DEC.From this work and earlier published results it appears that both axial and equatorial N-CH3 bonds in DEC are acceptable for activity.
