5429-01-6 Usage
Uses
Used in Organic Synthesis:
4-methylquinolin-6-ol is used as a key intermediate in the synthesis of various organic compounds due to its unique structure and reactivity.
Used in Biological Applications:
As a fluorescent probe, 4-methylquinolin-6-ol is utilized for labeling and tracking biological molecules, enabling researchers to study their behavior and interactions within complex systems.
Used in Pharmaceutical Production:
Leveraging its antimicrobial and antifungal properties, 4-methylquinolin-6-ol is employed in the development and production of pharmaceuticals to combat infections and diseases.
Used in Dye Manufacturing:
The strong fluorescent property of 4-methylquinolin-6-ol makes it suitable for use in the creation of dyes for various applications, including textiles and other industrial processes.
Used in Plastic Additives:
4-methylquinolin-6-ol is incorporated into plastic additives to enhance their properties, such as resistance to microbial degradation and improved fluorescence for specific applications.
Used in Drug Development:
4-methylquinolin-6-ol's potential in new drug development is being explored, particularly for its antimicrobial and antifungal activities, which could lead to the creation of novel therapeutic agents.
Used in Chemical Research:
4-methylquinolin-6-ol serves as a valuable tool in chemical research, providing insights into the synthesis and properties of quinoline derivatives and their potential applications in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 5429-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5429-01:
(6*5)+(5*4)+(4*2)+(3*9)+(2*0)+(1*1)=86
86 % 10 = 6
So 5429-01-6 is a valid CAS Registry Number.
5429-01-6Relevant academic research and scientific papers
Expansion of the aromatic part of Cinchona alkaloids. Annulation of quinolines with phenoxazine motifs
W?sińska-Ka?wa, Ma?gorzata,Giurg, Miros?aw,Boratyński, Przemys?aw J.,Skar?ewski, Jacek
supporting information, p. 308 - 315 (2017/12/08)
An oxidative cross-coupling strategy for quinoline ring annulation in Cinchona alkaloids has been developed. Key-reaction optimization by changing oxidants and adjusting the nucleophilicity of the 2-aminophenols led to cupreine and cupreidine expanded with the phenoxazinone unit in 56–75% yield. The stereochemical integrity of the obtained alkaloid structures was confirmed by combined experimental and computed CD and NMR data. The conformational study revealed a fast equilibrium of the three conformers, differing in the orientation of the pyrido[a-3,2]phenoxazine moiety.
AN IMPROVED PROCESS FOR THE SYNTHESIS OF QUINOLINE DERIVATIVES
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Page/Page column 8, (2008/06/13)
The present invention provides an improved process for the synthesis of quinoline derivatives. More particularly the present invention provides an improved and economical process for the synthesis of quinoline derivatives by the reaction of aniline/substituted anilines using two different catalysts, ferric chloride and zinc chloride in a one-pot set up reaction.
Process for the synthesis of quinoline derivatives
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Page/Page column 3, (2010/11/27)
The present invention provides an improved process for the synthesis of quinoline derivatives. More particularly the present invention provides an improved and economical process for the synthesis of quinoline derivatives by the reaction of aniline/substituted anilines using two different catalysts, ferric chloride and zinc chloride in a one-pot set up reaction.
