67525-28-4 Usage
Uses
Used in Pharmaceutical Research:
2-Chloro-3-ethylquinoline is utilized as a building block in the development of new drugs, contributing to the advancement of pharmaceuticals with its unique chemical structure and potential biological activities.
Used in Organic Synthesis:
As a key component in organic synthesis, 2-chloro-3-ethylquinoline aids in the creation of various chemical compounds, expanding the scope of chemical research and development.
Used in Agrochemical Development:
2-Chloro-3-ethylquinoline may also have applications in the development of new agrochemicals, potentially contributing to more effective and targeted agricultural solutions.
Used in Antibacterial Applications:
2-CHLORO-3-ETHYLQUINOLINE has been studied for its antibacterial properties, making it a candidate for use in applications that require bacterial inhibition or control.
Used in Antimalarial Applications:
With its potential antimalarial properties, 2-chloro-3-ethylquinoline could be employed in the development of treatments for malaria, a significant global health concern.
Check Digit Verification of cas no
The CAS Registry Mumber 67525-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,2 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67525-28:
(7*6)+(6*7)+(5*5)+(4*2)+(3*5)+(2*2)+(1*8)=144
144 % 10 = 4
So 67525-28-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClN/c1-2-8-7-9-5-3-4-6-10(9)13-11(8)12/h3-7H,2H2,1H3
67525-28-4Relevant academic research and scientific papers
Iron-Catalyzed Amination of Strong Aliphatic C(sp3)-H Bonds
Das, Sandip Kumar,Roy, Satyajit,Khatua, Hillol,Chattopadhyay, Buddhadeb
, p. 16211 - 16217 (2020/10/26)
A concept for intramolecular denitrogenative C(sp3)-H amination of 1,2,3,4-tetrazoles bearing unactivated primary, secondary, and tertiary C-H bonds is discovered. This catalytic amination follows an unprecedented metalloradical activation mechanism. The utility of the method is showcased with the short synthesis of a bioactive molecule. Moreover, an initial effort has been embarked on for the enantioselective C(sp3)-H amination through the catalyst design. Collectively, this study underlines the development of C(sp3)-H bond functionalization chemistry that should find wide application in the context of drug discovery and natural product synthesis.
Synthesis and 5-Hydroxytryptamine Antagonist Activity of 2-thio>-3-phenylquinoline and Its Analogues
Blackburn, Thomas P.,Cox, Barry,Guildford, Allen J.,Count, David J. Le,Middlemiss, Derek N.,et al.
, p. 2252 - 2259 (2007/10/02)
A series of 2-quinolines substituted at the 3-position with alkyl, aryl, or heteroaryl groups has been prepared in the search for novel and selective 5-HT2 antagonists.The affinity of the compounds for 5-HT1 recep
