939-17-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloroquinolin-2-one is used as a building block for the synthesis of various pharmaceuticals due to its potential anti-cancer and anti-inflammatory properties. It is valued for its ability to inhibit certain enzymes and biological processes, contributing to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Chloroquinolin-2-one serves as a key component in the creation of compounds with pesticidal or herbicidal activities, leveraging its chemical properties to enhance crop protection and yield.
Used in Organic Compounds Synthesis:
3-Chloroquinolin-2-one is utilized as an intermediate in the synthesis of a wide range of organic compounds, showcasing its versatility and applicability across various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 939-17-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 939-17:
(5*9)+(4*3)+(3*9)+(2*1)+(1*7)=93
93 % 10 = 3
So 939-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H6ClNO/c10-7-5-6-3-1-2-4-8(6)11-9(7)12/h1-5H,(H,11,12)
939-17-3Relevant academic research and scientific papers
One-pot copper-catalyzed three-component reaction: A modular approach to functionalized 2-quinolones
Kim, Ah Reum,Lim, Hee Nam
, p. 7855 - 7866 (2020/03/11)
A copper-catalyzed three-component annulation for the synthesis of functionalized 2-quinolones was developed. Three reactions including an SN2, a Knoevenagel, and finally C-N bond formation are involved in the designed cascade reaction using 2-bromoacylarenes, 2-iodoacetamide, and nucleophiles as the three components. A new catalytic system was discovered during the study and this modular approach is highly efficient to access functionalized 2-quinolone derivatives, compatible with a broad range of functional groups, scalable, and step-economic. Further derivatization of the obtained product demonstrates the synthetic utility of this method.
