65887-62-9 Usage
Uses
Used in Organic Synthesis:
8-Nitro-3,4-dihydroquinolin-2(1H)-one is used as a building block for the synthesis of complex organic molecules. Its unique structure and functional groups make it a valuable intermediate in the creation of a wide range of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 8-Nitro-3,4-dihydroquinolin-2(1H)-one is utilized as a precursor for the development of new drugs. The presence of the nitro group allows for further chemical modifications, which can lead to the discovery of novel bioactive compounds with potential therapeutic applications.
Used in the Synthesis of Bioactive Molecules:
8-Nitro-3,4-dihydroquinolin-2(1H)-one is employed as a starting material for the synthesis of bioactive molecules. Its chemical properties facilitate the production of compounds that can interact with biological targets, offering new avenues for the treatment of various diseases and conditions.
Overall, 8-Nitro-3,4-dihydroquinolin-2(1H)-one is a versatile compound with significant applications across the fields of organic synthesis and pharmaceutical research, making it a valuable asset for scientists and researchers in these domains.
Check Digit Verification of cas no
The CAS Registry Mumber 65887-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65887-62:
(7*6)+(6*5)+(5*8)+(4*8)+(3*7)+(2*6)+(1*2)=179
179 % 10 = 9
So 65887-62-9 is a valid CAS Registry Number.
65887-62-9Relevant academic research and scientific papers
A new efficient synthesis of 6-nitroquipazine
Lee, Byoung Se,Lee, Byung Chul,Jun, Jong-Gab,Chi, Dae Yoon
, p. 2637 - 2641 (2007/10/03)
A convenient and regioselective synthesis of 6-nitroquipazine from hydrocarbostyril in three steps is described. This synthetic route involved a nitration, a chlorination followed by aromatization, and an aromatic substitution reaction.
