21617-20-9 Usage
Uses
Used in Pharmaceutical Industry:
6-Chloro-2,3-Dihydroquinolin-4(1H)-One is used as a building block for the synthesis of bioactive compounds and drugs due to its versatile chemical structure and potential therapeutic properties.
Used as an Anti-Inflammatory Agent:
In the pharmaceutical industry, 6-Chloro-2,3-Dihydroquinolin-4(1H)-One is used as an anti-inflammatory agent, leveraging its ability to reduce inflammation and alleviate associated symptoms.
Used as an Analgesic:
6-Chloro-2,3-Dihydroquinolin-4(1H)-One is utilized as an analgesic, helping to relieve pain by interacting with specific pain pathways in the body.
Used as an Antimicrobial Agent:
6-Chloro-2,3-Dihydroquinolin-4(1H)-One is employed as an antimicrobial agent, exhibiting properties that can inhibit the growth of or kill microorganisms, thus serving as a potential treatment for infections.
Used as an Anticancer Agent:
6-Chloro-2,3-Dihydroquinolin-4(1H)-One is used as an anticancer agent, showing promise in the development of drugs that target and combat cancer cells.
Used in Enzyme Inhibition:
6-Chloro-2,3-Dihydroquinolin-4(1H)-One is investigated for its potential as an enzyme inhibitor, which can be crucial in regulating various biological processes and treating enzyme-related disorders.
Used in Cellular Process Modulation:
6-Chloro-2,3-Dihydroquinolin-4(1H)-One is also studied for its potential to modulate specific cellular processes, which can be instrumental in understanding and treating a range of diseases at the cellular level.
Check Digit Verification of cas no
The CAS Registry Mumber 21617-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,1 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21617-20:
(7*2)+(6*1)+(5*6)+(4*1)+(3*7)+(2*2)+(1*0)=79
79 % 10 = 9
So 21617-20-9 is a valid CAS Registry Number.
21617-20-9Relevant academic research and scientific papers
Trifluoromethanesulfonic acid catalyzed Friedel-Crafts acylation of aromatics with β-lactams
Anderson, Kevin W.,Tepe, Jetze J.
, p. 8475 - 8481 (2007/10/03)
N-Protected and unprotected 2-azetidinones, protolytically activated by superacidic trifluoromethanesulfonic acid, react with aromatic compounds to give β-amino aromatic ketones in good to excellent yields (65-98%). Non-benzenoid aromatics (pyrrole and ferrocene) produced good yield (64-89%) of the corresponding ketones.
