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3-(3,4-dimethoxyphenyl)quinolin-2(1H)-one is a complex organic compound with the molecular formula C18H15NO4. It is characterized by a quinolinone core, which is a derivative of quinoline with a carbonyl group at the 2-position. The compound features a 3,4-dimethoxyphenyl group attached to the quinoline nucleus, which contributes to its chemical properties and potential applications. This specific arrangement of atoms and functional groups may be relevant in the fields of medicinal chemistry and materials science, where such compounds are often studied for their biological activities or physical properties.

4970-03-0

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4970-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4970-03-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4970-03:
(6*4)+(5*9)+(4*7)+(3*0)+(2*0)+(1*3)=100
100 % 10 = 0
So 4970-03-0 is a valid CAS Registry Number.

4970-03-0Downstream Products

4970-03-0Relevant academic research and scientific papers

Palladium-Catalyzed Reductive Aminocarbonylation of Benzylammonium Triflates with o-Nitrobenzaldehydes for the Synthesis of 3-Arylquinolin-2(1 H)-ones

Liu, Yongzhu,Qi, Xinxin,Wu, Xiao-Feng

, p. 13824 - 13832 (2021/10/12)

A palladium-catalyzed straightforward procedure for the synthesis of 3-arylquinolin-2(1H)-ones has been developed. The synthesis proceeds through a palladium-catalyzed reductive aminocarbonylation reaction of benzylic ammonium triflates with o-nitrobenzaldehydes, and a wide range of 3-arylquinolin-2(1H)-ones was obtained in moderate to good yields with very good functional group compatibility.

Metal-free ring expansion of indoles with nitroalkenes: A simple, modular approach to 3-substituted 2-quinolones

Aksenov, Alexander V.,Smirnov, Alexander N.,Aksenov, Nicolai A.,Aksenova, Inna V.,Matheny, Jonathon P.,Rubin, Michael

, p. 8647 - 8656 (2015/03/03)

3-Substituted 2-quinolones are obtained via a novel metal-free transannulation reaction of 2-nitroolefins with 2-substituted indoles in polyphosphoric acid. This acid-mediated cascade transformation operates via the ANRORC (Addition of Nucleophile, Ring Opening, and Ring Closure) mechanism and can be used in combination with the Fisher indole synthesis to offer a practical three-component hetero-annulation approach to 2-quinolones from arylhydrazines, 2-nitroalkenes, and acetophenone. An alternative entry to this chemistry employing the alkylation of electron-rich arenes and hetarenes with 1-(2-indolyl)-2-nitroalkene has also been demonstrated.

Highly efficient modular metal-free synthesis of 3-substituted 2-quinolones

Aksenov, Alexander V.,Smirnov, Alexander N.,Aksenov, Nicolai A.,Aksenova, Inna V.,Bijieva, Asiyat S.,Rubin, Michael

supporting information, p. 9786 - 9788 (2014/12/12)

A modular approach to 3-substituted 2-quinolones via a cascade annulation reaction between 4-nitroketones and hydrazines has been developed.

Metal-free transannulation reaction of indoles with nitrostyrenes: A simple practical synthesis of 3-substituted 2-quinolones

Aksenov, Alexander V.,Smirnov, Alexander N.,Aksenov, Nicolai A.,Aksenova, Inna V.,Frolova, Liliya V.,Kornienko, Alexander,Magedov, Igor V.,Rubin, Michael

supporting information, p. 9305 - 9307 (2013/10/01)

3-Substituted 2-quinolones are obtained via a novel, metal-free transannulation reaction of 2-substituted indoles with 2-nitroalkenes in polyphosphoric acid. The reaction can be used in conjunction with the Fisher indole synthesis offering a practical three-component heteroannulation methodology to produce 2-quinolones from arylhydrazines, 2-nitroalkenes and acetophenone.

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