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2-Propen-1-one, 1-(4-methoxyphenyl)-3-(2-quinolinyl)-, also known as 1-(4-methoxyphenyl)-3-(2-quinolinyl)-2-propen-1-one, is a complex organic compound with the molecular formula C18H15NO2. It is characterized by a 2-propen-1-one backbone, which is a three-carbon chain with a carbonyl group at one end and a double bond at the other. The compound features a 4-methoxyphenyl group, which is a phenyl ring (a six-carbon ring with alternating double bonds) substituted with a methoxy group (-OCH3) at the 4-position. Additionally, it has a 2-quinolinyl group, which is a quinoline ring system (a bicyclic structure consisting of a benzene ring fused to a pyridine ring) attached at the 2-position. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly those with biological activity.

4401-04-1

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4401-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4401-04-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4401-04:
(6*4)+(5*4)+(4*0)+(3*1)+(2*0)+(1*4)=51
51 % 10 = 1
So 4401-04-1 is a valid CAS Registry Number.

4401-04-1Relevant academic research and scientific papers

In vitro and in vivo efficacy and in vitro metabolism of 1-phenyl-3-aryl-2-propen-1-ones against Plasmodium falciparum

Gutteridge, Clare E.,Nichols, Daniel A.,Curtis, Sean M.,Thota, Darshan S.,Vo, Joseph V.,Gerena, Lucia,Montip, Gettayacamin,Asher, Constance O.,Diaz, Damaris S.,DiTusa, Charles A.,Smith, Kirsten S.,Bhattacharjee, Apurba K.

, p. 5682 - 5686 (2006)

Investigation of a series of 1-phenyl-3-aryl-2-propen-1-ones resulted in the identification of nine inhibitors with submicromolar efficacy against at least one Plasmodium falciparum strain in vitro. These inhibitors were inactive when given orally in a Pl

Rapid Construction of Structurally Diverse Quinolizidines, Indolizidines, and Their Analogues via Ruthenium-Catalyzed Asymmetric Cascade Hydrogenation/Reductive Amination

Chen, Ya,He, Yan-Mei,Zhang, Shanshan,Miao, Tingting,Fan, Qing-Hua

supporting information, p. 3809 - 3813 (2019/01/14)

A rapid construction of enantioenriched benzo-fused quinolizidines, indolizidines, and their analogues by ruthenium-catalyzed asymmetric cascade hydrogenation/reductive amination of quinolinyl- and quinoxalinyl-containing ketones has been developed. This

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