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3-Acetylamino-6-chloro-4-phenyl-1H-quinolin-2-one is a complex organic compound with the molecular formula C19H14ClNO2. It is a derivative of quinolinone, a heterocyclic compound with a quinoline ring fused to a ketone group. This specific compound features a 3-acetylamino group, a 6-chloro substituent, and a 4-phenyl group attached to the quinoline core. It is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of various pharmaceuticals and agrochemicals. The compound's structure and properties make it a subject of interest for researchers exploring new drug candidates and chemical intermediates.

2854-15-1

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2854-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2854-15-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,5 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2854-15:
(6*2)+(5*8)+(4*5)+(3*4)+(2*1)+(1*5)=91
91 % 10 = 1
So 2854-15-1 is a valid CAS Registry Number.

2854-15-1Relevant 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

supporting information; experimental part, p. 3787 - 3789 (2009/04/06)

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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