13669-60-8 Usage
Uses
Used in Pharmaceutical Industry:
6-Methoxyquinoline-3-carboxaldehyde is used as a key intermediate in the synthesis of various quinoline and quinoxaline derivatives. These derivatives have been found to possess significant antimalarial activity, making 6-METHOXYQUINOLINE-3-CARBOXALDEHYDE an important contributor to the development of new drugs for the treatment of malaria.
Used in Chemical Synthesis:
In the field of organic chemistry, 6-methoxyquinoline-3-carboxaldehyde serves as a versatile reagent for the synthesis of a wide range of complex organic molecules. Its unique structure allows for various chemical reactions, such as condensation, substitution, and reduction, which can be utilized to create novel compounds with potential applications in various industries.
Used in Research and Development:
6-Methoxyquinoline-3-carboxaldehyde is also used in research and development laboratories for the study of its chemical properties and potential applications. Scientists and researchers can use 6-METHOXYQUINOLINE-3-CARBOXALDEHYDE to explore new synthetic routes, investigate its reactivity with other molecules, and develop new methods for its synthesis and purification.
Check Digit Verification of cas no
The CAS Registry Mumber 13669-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,6 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13669-60:
(7*1)+(6*3)+(5*6)+(4*6)+(3*9)+(2*6)+(1*0)=118
118 % 10 = 8
So 13669-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c1-14-10-2-3-11-9(5-10)4-8(7-13)6-12-11/h2-7H,1H3
13669-60-8Relevant academic research and scientific papers
Enantioselective synthesis of substituted 3-quinolyl alkanols and their application to asymmetric autocatalysis
Sato, Itaru,Nakao, Tomohiko,Sugie, Rie,Kawasaki, Tsuneomi,Soai, Kenso
, p. 1419 - 1428 (2007/10/03)
Enantioenriched 3-quinolyl alkanols act as asymmetric autocatalysts in the addition of diisopropylzinc to the corresponding substituted quinoline-3-carbaldehydes, to afford themselves with an amplified enantiomeric excess (ee) of up to 97%.
