製品名:6-chloro-2-methyl-1H-pyrrolo[2,3-b]pyridine

IUPAC Name:6-chloro-2-methyl-1H-pyrrolo[2,3-b]pyridine

CAS番号:872366-91-1
分子式:C8H7ClN2
純度:95%+
カタログ番号:CM460060
分子量:166.61

包装単位 有効在庫 価格(USD) 数量
CM460060-100mg in stock ǜȬũ
CM460060-250mg in stock ưưț
CM460060-10g in stock ƦƦȬƎ

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製品詳細

CAS番号:872366-91-1
分子式:C8H7ClN2
融点:-
SMILESコード:CC1=CC2=C(N1)N=C(Cl)C=C2
密度:
カタログ番号:CM460060
分子量:166.61
沸点:
MDL番号:MFCD12924462
保管方法:

Category Infos

Azaindoles
Azaindole can be regarded as the biological isostere of indole, and the molecular unit of indole plays a huge role in the life process. Many drug molecules contain indole units. Azaindole is an important heterocyclic intermediate with good biological and medicinal value, and is the core structure of many drugs, such as antitumor drugs, dopamine D4 receptors, kinase inhibitors, thrombin inhibitors, etc. Therefore, it has a wide range of application value in medical research. Azaindole can be regarded as the biological isostere of indole, and the molecular unit of indole plays a huge role in the life process. Many drug molecules contain indole units. Azaindole is an important heterocyclic intermediate with good biological and medicinal value, and is the core structure of many drugs, such as antitumor drugs, dopamine D4 receptors, kinase inhibitors, thrombin inhibitors, etc. Therefore, it has a wide range of application value in medical research.Azaindole

Product Other Information

Product Overview 6-Chloro-2-methyl-1h-pyrrolo[2,3-b]pyridine is a chemical compound that has been studied for its potential applications in scientific research.
Synthesis Method One method involves the reaction of 2-methylpyridine with 1,3-dichloro-1,3-butadiene in the presence of a catalyst. Another method involves the reaction of 6-chloropyridine-2-carbaldehyde with methylamine and an alkylating agent. These methods have been optimized to produce high yields of the compound with minimal impurities.
Synthesis and Application It has been found to have anticancer properties and has been tested for its ability to inhibit the growth of cancer cells. Additionally, this compound has been studied for its potential as a treatment for neurological disorders such as Alzheimer's disease and Parkinson's disease.
Future Directions One potential direction is to explore its potential as a treatment for neurological disorders such as Alzheimer's disease and Parkinson's disease. Additionally, further research could be done to optimize the synthesis method of this compound to produce higher yields with minimal impurities. Finally, research could be done to better understand the mechanism of action of this compound, which could lead to the development of more effective treatments for a variety of diseases.