209353-22-0 Usage
Uses
Used in Pharmaceutical Industry:
6-Quinolinol,8-fluoro-(9CI) serves as a crucial building block in the synthesis of various pharmaceutical compounds. Its unique structure, including the presence of a fluorine atom, contributes to the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 6-Quinolinol,8-fluoro-(9CI) is employed for studying the effects of fluorination on the properties and reactivity of quinoline derivatives. This research aids in understanding the structure-activity relationships and can lead to the discovery of novel compounds with improved pharmacological profiles.
Used in Drug Development:
6-Quinolinol,8-fluoro-(9CI) may have potential therapeutic properties, and its exploration in drug development can lead to the creation of new medications. Further research is necessary to determine its biological activity, efficacy, and safety in treating specific medical conditions.
While the provided materials do not explicitly mention different applications in various industries, the above uses highlight the compound's significance in the pharmaceutical industry, chemical research, and drug development. Further exploration and research could potentially reveal additional applications in other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 209353-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,3,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 209353-22:
(8*2)+(7*0)+(6*9)+(5*3)+(4*5)+(3*3)+(2*2)+(1*2)=120
120 % 10 = 0
So 209353-22-0 is a valid CAS Registry Number.
209353-22-0Relevant academic research and scientific papers
Stadlwieser, Josef,Barbier, Pierre,Taylor, Sven
, p. 1088 - 1094 (1998)
8-Fluoro-6-(methoxymethoxy)quinoline (1) was synthesized, and the reactivity of 1 against organolithium compounds was studied under different reaction conditions. With BuLi, directed ortho-metalation (DoM) was accompanied by 1,2-addition to the C=N bond.
