96600-76-9 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone is used as a building block in the pharmaceutical industry for the synthesis of various drugs. Its unique structure and functional groups make it a valuable component in the development of new therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone is utilized as an intermediate in the preparation of pharmaceutical and fine chemical products. Its presence in these compounds contributes to their biological activities and therapeutic potential.
Used in Drug Discovery:
4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone is employed in drug discovery processes to explore its potential as a lead compound for the development of new medications. Its biological activities and chemical properties make it a promising candidate for further research and optimization.
Used in Fine Chemical Production:
4-Chloro-3-forMyl-1-Methyl-2(1H)-quinolinone is also used in the production of fine chemicals, where its unique structure and functional groups contribute to the properties and applications of the final products. Its versatility in chemical reactions allows for the synthesis of a wide range of specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 96600-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,0 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96600-76:
(7*9)+(6*6)+(5*6)+(4*0)+(3*0)+(2*7)+(1*6)=149
149 % 10 = 9
So 96600-76-9 is a valid CAS Registry Number.
96600-76-9Relevant academic research and scientific papers
Nucleophilic Chlorination of 3-Formyl-4-hydroxy-quinolin-2(1H)-ones
Fiala, Werner,Stadlbauer, Wolfgang
, p. 128 - 134 (2007/10/02)
Chlorination of 1-substituted 3-formyl-4-hydroxy-2-quinolones (1a, b) with phosphorylchloride leads to 4-chloro-3-dichloromethylquinolones (2), which can be hydrolyzed to 4-chloro-3-formylquinolones (4).From the anilinomethylene quinolinediones (3), at lo
Organic Azides in Heterocyclic Synthesis, 12. Thermal Cyclization of 4-Azido-3-formyl-2-quinolones to Isoxazoloquinolones
Roschger, Peter,Stadlbauer, Wolfgang
, p. 401 - 403 (2007/10/02)
Thermolysis of the 4-azido-3-formyl-2-quinolone 6, which was prepared from the 4-hydroxy-2-quinolone 1, afforded the ring-closed isoxazoloquinolone 7. 3-(Arylaminomethylene)-2,4-quinolinediones 2 could not be transformed into an azide precursor in order t
Chemistry of Carbostyril: Part I - Oxidation Reactions of 4-Hydroxy- and 4-Hydroxy-1-methyl-2(1H)-quinolinones
Khan, Khalid A.,Shoeb, Aboo
, p. 62 - 66 (2007/10/02)
4-Hydroxy-2(1H)-quinolinone (1) reacts with acetic anhydride in dimethylsulphoxide at 100 deg to afford 3-dimethylsulfonioquinoline-2,4-dionate (3) whereas 3,3'-methylenebis (4) and 2,3,4,5,1',2',3',4'-octahydro-4,2',4'-trioxospioroquinoline-2,3'-quinoline> (5) are formed when the reaction is carried out at 165-70 deg.The involvement of 4 as a precursor of 5 has been demonstrated.Probable mechanisms of their formation have been proposed.The behaviour of 4-hydroxy-1-methyl-2(1H)-quinolinone (2) towards other oxidising agents, such as HNO3, CrO3, SOCl2-DMF and p-benzoquinone has also been studied.
