296759-28-9 Usage
Uses
Used in Agrochemical Industry:
2-Chloro-6,8-dinitroquinoline is used as an intermediate in the production of agrochemicals for its ability to contribute to the development of effective pesticides. Its chemical properties allow for the creation of compounds that can protect crops from pests and diseases, thereby enhancing agricultural productivity.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Chloro-6,8-dinitroquinoline serves as a key intermediate in the synthesis of various drugs. Its bacteriostatic and anti-inflammatory properties make it a valuable component in the development of medications aimed at treating bacterial infections and inflammatory conditions.
Used in Organic Synthesis:
2-Chloro-6,8-dinitroquinoline is utilized as a building block in the synthesis of a wide range of organic compounds. Its unique structure allows chemists to create diverse molecules with specific functionalities, which can be applied across various fields, including materials science, chemical research, and specialty chemical production.
Check Digit Verification of cas no
The CAS Registry Mumber 296759-28-9 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 296759-28:
(8*2)+(7*9)+(6*6)+(5*7)+(4*5)+(3*9)+(2*2)+(1*8)=209
209 % 10 = 9
So 296759-28-9 is a valid CAS Registry Number.
296759-28-9Relevant academic research and scientific papers
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.
