Nombre del producto:6-chloroisoindolin-5-amine

IUPAC Name:6-chloro-2,3-dihydro-1H-isoindol-5-amine

CAS:905273-33-8
Fórmula molecular:C8H9ClN2
Pureza:95%
Número de catálogo:CM149088
Peso molecular:168.62

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Detalles del producto

Núm. De CAS :905273-33-8
Fórmula molecular:C8H9ClN2
Punto de fusión:-
Código de sonrisas:NC1=CC2=C(CNC2)C=C1Cl
Densidad:
Número de catálogo:CM149088
Peso molecular:168.62
Punto de ebullición:
Nº Mdl:
Almacenamiento:Store at 2-8°C.

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Product Overview 6-Chloroisoindolin-5-amine is a chemical compound that has gained significant attention in scientific research due to its potential applications in various fields. It is a heterocyclic organic compound that contains a chlorine atom attached to an isoindoline ring. This compound has been synthesized using various methods, and its unique structure has made it an attractive target for research.
Synthesis and Application The synthesis of 6-Chloroisoindolin-5-amine can be achieved through various methods. One of the most common methods involves the reaction of 5-aminoisoindoline with thionyl chloride and hydrogen chloride gas. This reaction results in the formation of 6-chloroisoindolin-5-amine as the final product. 6-Chloroisoindolin-5-amine has been extensively studied for its potential applications in various scientific fields. One of the most significant applications of this compound is in medicinal chemistry. It has been shown to exhibit potent anti-cancer activity against various cancer cell lines. This compound has also been studied for its potential use as a therapeutic agent for the treatment of neurodegenerative diseases.
Future Directions There are several future directions for research on 6-Chloroisoindolin-5-amine. One potential direction is to further investigate its mechanism of action in cancer cells. This could lead to the development of more potent anti-cancer agents. Another potential direction is to study its potential use as a therapeutic agent for the treatment of neurodegenerative diseases. Finally, research could focus on developing new methods for synthesizing this compound, which could lead to more efficient and cost-effective production.