cas 627531-51-5|| where to buy 6-Aminoquinoline-2-carbonitrile

Nombre del producto:6-Aminoquinoline-2-carbonitrile

IUPAC Name:6-aminoquinoline-2-carbonitrile

: CAS：627531-51-5; Fórmula molecular：C10H7N3; Pureza：97%

: Número de catálogo：CM238986; Peso molecular：169.19

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CM238986-1g	in stock	ȖŪŞ

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Detalles del producto

: Núm. De CAS :627531-51-5; Fórmula molecular:C10H7N3; Punto de fusión:-; Código de sonrisas:N#CC1=NC2=CC=C(N)C=C2C=C1; Densidad:

: Número de catálogo:CM238986; Peso molecular:169.19; Punto de ebullición:; Nº Mdl:; Almacenamiento:

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.

Product Other Information

Product Overview	6-Aminoquinoline-2-carbonitrile, also known as 6-AQC, is an organic compound that has been used for a variety of scientific research applications. It is a colorless, crystalline solid with a molecular weight of 169.19 g/mol. 6-AQC has been found to have a wide range of biological activities due to its unique structure, which consists of an aromatic ring, a nitrogen atom and a carbonitrile group. 6-AQC has been used in a variety of research applications, including as a substrate for enzyme-catalyzed reactions, as a reactant in organic synthesis, and as an inhibitor of enzyme activity.
Synthesis and Application	6-Aminoquinoline-2-carbonitrile can be synthesized using a variety of methods, including the use of aryl halides, aryl amines, and aryl carbonitriles. The most common method of synthesis is the reaction of aryl halides with aqueous ammonia. This reaction yields a secondary amine, which can then be reacted with a carbonitrile to form 6-Aminoquinoline-2-carbonitrile. The reaction is usually carried out in aqueous solution at room temperature and is usually complete within minutes. 6-Aminoquinoline-2-carbonitrile has been used for a variety of scientific research applications. It has been used as a substrate for enzyme-catalyzed reactions, as a reactant in organic synthesis, and as an inhibitor of enzyme activity. 6-Aminoquinoline-2-carbonitrile has also been used to study the structure and function of proteins, as well as the structure and function of cell membranes. In addition, 6-Aminoquinoline-2-carbonitrile has been used to study the pharmacology of drugs, as well as to study the effects of environmental pollutants on organisms.
Future Directions	There are a number of potential future directions for the use of 6-Aminoquinoline-2-carbonitrile. One potential direction is the development of new synthetic methods for the synthesis of 6-Aminoquinoline-2-carbonitrile. Additionally, further research could be conducted to investigate the mechanism of action of 6-Aminoquinoline-2-carbonitrile, as well as its effects on the nervous system and other physiological systems. Finally, 6-Aminoquinoline-2-carbonitrile could be explored as a potential therapeutic agent, as it has been found to have a variety of biochemical and physiological effects.