6285-79-6 Usage
Description
A quinoline derivative with a 4-methoxyphenyl group and an ethyl chain attached to the quinoline ring.
Applications
Used in research and pharmaceutical applications.
Functions as a fluorescent probe for studying protein-protein interactions.
Investigated for potential therapeutic properties, including anti-tumor and anti-inflammatory activities.
Pharmacological Properties
Influence of the 4-methoxyphenyl group on pharmacokinetics and pharmacodynamics.
Significance
Interest in drug development and medicinal chemistry studies due to its pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6285-79-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6285-79:
(6*6)+(5*2)+(4*8)+(3*5)+(2*7)+(1*9)=116
116 % 10 = 6
So 6285-79-6 is a valid CAS Registry Number.
6285-79-6Relevant articles and documents
Nickel-Catalyzed Dehydrogenation of N-Heterocycles Using Molecular Oxygen
Banerjee, Debasis,Bera, Atanu,Bera, Sourajit
, (2020/09/02)
Herein, an efficient and selective nickel-catalyzed dehydrogenation of five- and six-membered N-heterocycles is presented. The transformation occurs in the presence of alkyl, alkoxy, chloro, free hydroxyl and primary amine, internal and terminal olefin, trifluoromethyl, and ester functional groups. Synthesis of an important ligand and the antimalarial drug quinine is demonstrated. Mechanistic studies revealed that the cyclic imine serves as the key intermediate for this stepwise transformation.
