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3-Amino-6-chloro-4-(2-chloro-phenyl)-1H-quinolin-2-one is a complex organic compound with the molecular formula C15H9Cl2N2O. It is a derivative of quinolinone, featuring a quinoline ring system with a 2-amino group at the 3-position, a chlorine atom at the 6-position, and a 2-chlorophenyl group attached at the 4-position. 3-Amino-6-chloro-4-(2-chloro-phenyl)-1H-quinolin-2-one is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its structure provides a foundation for further functionalization and modification, making it a valuable intermediate in the development of new compounds with specific biological activities.

5220-04-2

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5220-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5220-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5220-04:
(6*5)+(5*2)+(4*2)+(3*0)+(2*0)+(1*4)=52
52 % 10 = 2
So 5220-04-2 is a valid CAS Registry Number.

5220-04-2Upstream product

5220-04-2Downstream Products

5220-04-2Relevant academic research and scientific papers

Synthesis and in vitro anti-hepatitis B virus activities of 4-aryl-6-chloro-quinolin-2-one and 5-aryl-7-chloro-1,4-benzodiazepine derivatives

Cheng, Pi,Zhang, Quan,Ma, Yun-Bao,Jiang, Zhi-Yong,Zhang, Xue-Mei,Zhang, Feng-Xue,Chen, Ji-Jun

, p. 3787 - 3789 (2008)

A series of 4-aryl-6-chloro-quinolin-2-ones and 5-aryl-7-chloro-1,4-benzodiazepine were synthesized and assayed for their in vitro anti-hepatitis B virus activities and cytotoxicities for the first time. Some of the tested compounds were active against HBsAg and HBeAg secretion in Hep G2.2.15 cells. Compound 5c showed IC50 of 0.074 and 0.449 mM on HBsAg and HBeAg secretions, respectively, which were 10 times higher than that of its analog 4c and led to better selective index (SI) values (SI = 23.2 and 3.4, respectively).

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