64165-33-9 Usage
Uses
Used in Chelating Applications:
6-Quinolinol, 8-methylis used as a chelating agent for its ability to form stable complexes with metal ions. This property is valuable in various industrial and research applications where metal ion management is crucial.
Used in Antimicrobial Applications:
In the field of microbiology, 6-Quinolinol, 8-methylis utilized as an antimicrobial agent, serving in the production of antiseptic and disinfectant products to combat microbial growth and infection.
Used in Pharmaceutical Synthesis:
6-Quinolinol, 8-methylplays a pivotal role in the pharmaceutical industry, where it is used as a key intermediate in the synthesis of various drugs, contributing to the development of new therapeutic agents.
Used in Disease Treatment Research:
6-Quinolinol, 8-methylis studied for its potential use in the treatment of certain diseases, such as cancer and neurodegenerative disorders. Its metal-chelating ability is of particular interest, as it may help mitigate the effects of metal ions implicated in these disease processes.
Used in Chemical Research:
In the realm of chemical research, 6-Quinolinol, 8-methylserves as a subject of study for understanding its reactivity, stability, and potential applications in the development of new chemical compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 64165-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,6 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64165-33:
(7*6)+(6*4)+(5*1)+(4*6)+(3*5)+(2*3)+(1*3)=119
119 % 10 = 9
So 64165-33-9 is a valid CAS Registry Number.
64165-33-9Relevant academic research and scientific papers
Rh(iii)-Catalyzed mild straightforward synthesis of quinoline-braced cyclophane macrocycles: Via migratory insertion
Bera, Satabdi,Ghosh, Bidhan,Ghosh, Pintu,Samanta, Rajarshi
, p. 13134 - 13137 (2021/12/20)
An efficient Rh(iii)-catalyzed straightforward strategy is developed for the synthesis of quinoline braced cyclophane macrocycles via methyl (sp3) C-H functionalization. The method is mild, simple and regioselective with various ring sizes and has good fu
Multi-Functional Oxidase Activity of CYP102A1 (P450BM3) in the Oxidation of Quinolines and Tetrahydroquinolines
Li, Yushu,Wong, Luet L.
, p. 9551 - 9555 (2019/08/06)
Tetrahydroquinoline, quinoline, and dihydroquinolinone are common core motifs in drug molecules. Screening of a 48-variant library of the cytochrome P450 enzyme CYP102A1 (P450BM3), followed by targeted mutagenesis based on mutation-selectivity correlations from initial hits, has enabled the hydroxylation of substituted tetrahydroquinolines, quinolines, and 3,4-dihydro-2-quinolinones at most positions around the two rings in good to high yields at synthetically relevant scales (1.5 g L?1 day?1). Other oxidase activities, such as C?C bond desaturation, aromatization, and C?C bond formation, were also observed. The enzyme variants, with mutations at the key active site residues S72, A82, F87, I263, E267, A328, and A330, provide direct and sustainable routes to oxy-functionalized derivatives of these building block molecules for synthesis and drug discovery.
