Nombre del producto:4-(Aminomethyl)isoindolin-1-one

IUPAC Name:4-(aminomethyl)-2,3-dihydro-1H-isoindol-1-one

CAS:366453-27-2
Fórmula molecular:C9H10N2O
Pureza:95%+
Número de catálogo:CM238719
Peso molecular:162.19

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Detalles del producto

Núm. De CAS :366453-27-2
Fórmula molecular:C9H10N2O
Punto de fusión:-
Código de sonrisas:O=C1NCC2=C1C=CC=C2CN
Densidad:
Número de catálogo:CM238719
Peso molecular:162.19
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Isoindolinones
Isoindolinones are ubiquitous structural motifs in natural products and pharmaceuticals. Isoindolinones are precursors to other valuable building blocks.

Product Other Information

Product Overview 4-(Aminomethyl)isoindolin-1-one, commonly referred to as AMI, is an organic compound with a wide range of applications in scientific research.
Physical Properties The main advantage of using AMI in laboratory experiments is its high solubility in aqueous solutions, which allows for easy manipulation and handling.
Chemical Properties AMI is relatively stable and can be stored for long periods of time without significant degradation. However, AMI is also highly toxic and should be handled with care in the laboratory.
Synthesis and Application AMI has a wide range of applications in scientific research, including the synthesis of drugs, agricultural chemicals, and other compounds. It has also been used in the development of new materials, such as polymers and nanomaterials. In addition, AMI has been used in the synthesis of fluorescent probes and in the development of synthetic catalysts. Furthermore, AMI has been used in the synthesis of compounds with potential applications in drug discovery and development.
Synthesis Method The most common method is the condensation of ethyl acetoacetate and 4-aminobutyric acid in the presence of a base such as potassium carbonate or sodium hydroxide. This reaction is typically carried out at temperatures between 50-100°C and yields the desired product in high yield. Other methods for the synthesis of AMI include the reaction of ethyl acetoacetate and 4-aminobutyric acid with ammonia, and the reaction of ethyl acetoacetate and 4-aminobutyric acid with boron trifluoride.