Название продукции:(8-Fluoroquinolin-3-yl)boronic acid

IUPAC Name:(8-fluoroquinolin-3-yl)boronic acid

CAS:1207750-07-9
Молекулярная формула:C9H7BFNO2
Чистота:95%
Номер в каталоге:CM205864
Молекулярная масса:190.97

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Информация о продукции

Номер CAS:1207750-07-9
Молекулярная формула:C9H7BFNO2
Точка плавления:-
Smiles-код:FC1=C2N=CC(B(O)O)=CC2=CC=C1
Плотность:
Номер в каталоге:CM205864
Молекулярная масса:190.97
Точка кипения:
Номер Mdl:MFCD18382879
Хранение:

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.
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Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Product Other Information

Product Overview (8-Fluoroquinolin-3-yl)boronic acid, also known as 8FQB, is a boronic acid derivative that has been used in a variety of scientific research applications. 8FQB has been used in the synthesis of organic compounds, as a reagent in organic reactions, and as a tool to study enzyme-catalyzed reactions. In addition to its use in the laboratory, 8FQB has also been used to study biochemical and physiological processes in living organisms.
Physical Properties (8-Fluoroquinolin-3-yl)boronic acid is a white crystalline solid. It is not soluble in water and must be dissolved in an organic solvent before use.
Chemical Properties (8-Fluoroquinolin-3-yl)boronic acid has the main advantage for laboratory experiments is its relatively low cost and ease of synthesis. Additionally, (8-Fluoroquinolin-3-yl)boronic acid is relatively stable in aqueous solution and can be stored for extended periods of time. Additionally, it can be toxic if ingested, so it should be handled with care.
Synthesis and Application It has been used as a reagent in organic reactions, as a tool to study enzyme-catalyzed reactions, and as a tool to study the interactions between proteins and small molecules. (8-Fluoroquinolin-3-yl)boronic acid has also been used to study the structure and function of proteins, as well as to study the effects of drugs on biological systems.
Future Directions (8-Fluoroquinolin-3-yl)boronic acid could be used to further study the structure and function of proteins, as well as to study the effects of drugs on biological systems. It could be used to study the interactions between proteins and small molecules, and to study the effects of environmental factors on biological systems. Additionally, (8-Fluoroquinolin-3-yl)boronic acid could be used to develop new drugs or to study the effects of existing drugs on biological systems. Finally, It could be used to study the effects of metabolic processes on biological systems.