296759-27-8 Usage
Uses
Used in Chemical Synthesis:
6,8-DINITRO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used as a precursor in the synthesis of various organic compounds, playing a crucial role in the production of dyes, pharmaceuticals, and agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6,8-DINITRO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used as a building block for the development of new drugs, leveraging its potential biological activities.
Used in Agrochemical Industry:
6,8-DINITRO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used as a precursor in the formulation of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Dye Production:
6,8-DINITRO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used as a starting material in the production of dyes, where its chemical properties contribute to the creation of vibrant and stable colorants.
Used in Chemical Research:
As a reagent in chemical reactions, 6,8-DINITRO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is used for the formation of heterocyclic compounds, aiding researchers in advancing the field of organic chemistry.
Used in Biological Research:
6,8-DINITRO-3,4-DIHYDRO-1H-QUINOLIN-2-ONE is studied for its potential antibacterial and antitumor properties, serving as a subject of interest in biological research aimed at discovering new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 296759-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,7,5 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 296759-27:
(8*2)+(7*9)+(6*6)+(5*7)+(4*5)+(3*9)+(2*2)+(1*7)=208
208 % 10 = 8
So 296759-27-8 is a valid CAS Registry Number.
296759-27-8Relevant academic research and scientific papers
Medvedeva, A. Yu.,Yakunina,Atroshchenko, Yu. M.,Shumskii,Blokhin
, p. 1733 - 1737 (2011)
Dinitro derivatives of 8-oxyquinoline, 8-oxyquinaldine, and 3,4-dihydroquinolin-2-one when reacted with NaBH4 form hydride σH-adducts that are involved into a multicomponent Mannich reaction affording pyridoazabicyclo[3.3.1]nonane.
Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1
Lee, Byoung Se,Chu, Soyoung,Lee, Byung Chul,Chi, Dae Yoon,Choe, Yearn Seong,Jeong, Kyung Ja,Jin, Changbae
, p. 1559 - 1562 (2007/10/03)
6-Nitroquipazine has been known as one of the most potent and selective inhibitors of serotonin transporter in vitro and in vivo. Nine derivatives of 6-nitroquipazine were synthesized and tested for their potential abilities to displace [3H]citalopram binding to the rat cortical membranes. (C) 2000 Elsevier Science Ltd. All rights reserved.
