3954-50-5 Usage
Uses
Used in Pharmaceutical Industry:
6-Methoxy-1-methyl-2,3-dihydro-1H-quinolin-4-one is used as a potential treatment for depression due to its psychotomimetic effects similar to ketamine. It is being investigated for its ability to modulate neurotransmission and alleviate depressive symptoms.
Used in Pain Management:
6-Methoxy-1-methyl-2,3-dihydro-1H-quinolin-4-one is used as a potential pain reliever, as it has shown promise in providing analgesic effects. Its mechanism of action is still being studied, but it may involve modulation of the central nervous system.
Used in Neuroprotection:
6-Methoxy-1-methyl-2,3-dihydro-1H-quinolin-4-one is used as a potential neuroprotective agent, which may help protect neurons from damage and degeneration. Its neuroprotective properties are currently under investigation, and further research is needed to understand its full potential in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 3954-50-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,5 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3954-50:
(6*3)+(5*9)+(4*5)+(3*4)+(2*5)+(1*0)=105
105 % 10 = 5
So 3954-50-5 is a valid CAS Registry Number.
3954-50-5Relevant academic research and scientific papers
Formation of acridones by ethylene extrusion in the reaction of arynes with β-lactams and dihydroquinolinones
Fang, Yuesi,Rogness, Donald C.,Larock, Richard C.,Shi, Feng
, p. 6262 - 6270 (2012/09/22)
N-Unsubstituted β-lactams react with a molecule of aryne by insertion into the amide bond to form a 2,3-dihydroquinolin-4-one, which subsequently reacts with another molecule of aryne to form an acridone by extrusion of a molecule of ethylene. 2,3-Dihydroquinolin-4-ones react under the same reaction conditions to afford identical results. This is the first example of ethylene extrusion in aryne chemistry.
Palladium-catalyzed intramolecular nucleophilic substitution at the alkoxycarbonyl group
Sole, Daniel,Serrano, Olga
, p. 7270 - 7272 (2008/09/17)
(Chemical Equation Presented) Coaxed into action: Although ester groups are usually inert towards organopalladium reagents, β-(2-haloanilino)esters undergo intramolecular palladium-catalyzed acylation to give dihydroquinolin-4-ones (see scheme). A four-me
