cas 15912-68-2|| where to buy 6-Fluoro-2-methylquinolin-4-ol

Product Name:6-Fluoro-2-methylquinolin-4-ol

IUPAC Name:6-fluoro-2-methylquinolin-4-ol

: CAS：15912-68-2; Molecular Formula：C10H8FNO; Purity：97%

: Catalog Number：CM144224; Molecular Weight：177.18

Packing Unit	Available Stock	Price($)
CM144224-5g	in stock	ƎțŴ
CM144224-25g	in stock	țǊŴ

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Product Details

: CAS NO:15912-68-2; Molecular Formula:C10H8FNO; Melting Point:-; Smiles Code:CC1=NC2=C(C=C(F)C=C2)C(O)=C1; Density:

: Catalog Number:CM144224; Molecular Weight:177.18; Boiling Point:275.7°C at 760 mmHg; MDL No:MFCD00041442; Storage:Store at 2-8°C.

Category Infos

: Quinolines; Quinolines are an important class of biologically active heterocyclic compounds, and their derivatives usually exhibit a variety of biological activities. They can be used as antimalarial drugs and in the preparation of other antimalarial drugs. Other important activities of quinoline derivatives include inhibitory activity against EGFR-TK and antipsychotic activity. Futhermore, quinoline scaffolds are present in various drug molecules, including the antimalarial drugs aablaquine, chloroquine, mefloquine and primaquine, and the antibacterial agents gatifloxacin, levofloxacin, and moxifloxacin.; Quinoline Price; if you have any question on quinoline price, we will give the professional answers to your short questions.

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Product Other Information

Product Overview	6-Fluoro-2-methylquinolin-4-ol (6FMQ) is an organic compound belonging to the quinoline family of compounds. It has a wide range of applications in various fields, including synthetic organic chemistry, medicinal chemistry, and biochemistry. 6FMQ is a highly versatile compound, with its unique structure allowing for a wide range of chemical reactions. It has been studied for its potential applications in the fields of drug discovery, drug delivery, and drug metabolism.
Synthesis and Application	The synthesis of 6-Fluoro-2-methylquinolin-4-ol is typically achieved through a two-step reaction. The first step involves the condensation of 2-methylquinoline and 4-hydroxybenzoic acid in the presence of a base, such as sodium hydroxide. The second step involves the reaction of the intermediate product with fluoroacetic acid, resulting in the formation of 6-Fluoro-2-methylquinolin-4-ol. This method is simple and cost-effective, making it an attractive option for laboratory use.
Future Directions	The potential applications of 6-Fluoro-2-methylquinolin-4-ol are still being explored. Future research may focus on the development of new synthetic methods for the production of 6-Fluoro-2-methylquinolin-4-ol, as well as the development of new applications for the compound. In addition, future research may focus on the development of new methods for the delivery of 6-Fluoro-2-methylquinolin-4-ol, as well as the development of new methods for the measurement of its biological activity. Finally, future research may focus on the development of new methods for the identification and characterization of the biochemical and physiological effects of 6-Fluoro-2-methylquinolin-4-ol.