87602-55-9 Usage
Heterocyclic compound
Contains both quinoline and piperidine rings The compound has a complex structure with multiple interconnected rings, which include both carbon and nitrogen atoms.
Potential applications in medicinal chemistry
It is being studied for its possible use in the development of pharmaceutical drugs and biologically active molecules This means that the compound could have properties that make it useful in creating new medications or other compounds with therapeutic effects.
Building block in the synthesis of other organic compounds
It can be used as a starting material or intermediate in the creation of other complex organic molecules This property makes it valuable in organic chemistry research and development.
Ongoing research on biological activities and therapeutic uses
Scientists are actively studying this compound to better understand its properties and potential applications Further studies are needed to fully comprehend its potential benefits and possible uses in various fields.
Need for additional studies
Further research is necessary to fully understand the properties and potential applications of 2,8-dimethyl-4-(2-methylpiperidin-1-yl)quinoline This emphasizes the importance of continued investigation and experimentation to determine the compound's true potential.
Check Digit Verification of cas no
The CAS Registry Mumber 87602-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,0 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87602-55:
(7*8)+(6*7)+(5*6)+(4*0)+(3*2)+(2*5)+(1*5)=149
149 % 10 = 9
So 87602-55-9 is a valid CAS Registry Number.
87602-55-9Relevant articles and documents
New quinolines as potential CNS agents
Sathi,Gujrati,Sharma,Nath,Bhargava,Shanker
, p. 767 - 772 (2007/10/02)
The compounds 1a-1l and 2a-2m were synthesized by condensation of various aryl-1-(4-aminophenyl)piperazines and substituted piperidines with substituted 4-chloroquinolines. The compounds were screened for their monoamine oxidase (MAO) inhibitory activitie