Category: 33631-05-9

Share a compound : 33631-05-9

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,33631-05-9, its application will become more common.

Adding a certain compound to certain chemical reactions, such as: 33631-05-9, 2-Aminopyridin-4-ol, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, 33631-05-9, blongs to pyridine-derivatives compound. Product Details of 33631-05-9

2-Amino-4-hydroxypyridine (4.4 g, 40.0 mmol)After dissolving in 200 mL of EtOH,Chloroacetaldehyde (16.5 mL, 100 mmol) was added,Stir the mixture overnight.The reaction solution was concentrated on a column chromatography to give white solid 6 imidazo [1,2-a] pyridine-7-ol in 88% yield.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,33631-05-9, its application will become more common.

Reference:
Patent; East China Normal University; Hu Wenhao; Xi Jianbei; Lei Ruirui; Zhu Mengli; Ma Mingliang; Xiao Guolan; Zhang Xiongwen; Fang Yanfen; Li Hongyu; (28 pag.)CN106496222; (2017); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Share a compound : 33631-05-9

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,33631-05-9, its application will become more common.

Adding a certain compound to certain chemical reactions, such as: 33631-05-9, 2-Aminopyridin-4-ol, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, 33631-05-9, blongs to pyridine-derivatives compound. Product Details of 33631-05-9

2-Amino-4-hydroxypyridine (4.4 g, 40.0 mmol)After dissolving in 200 mL of EtOH,Chloroacetaldehyde (16.5 mL, 100 mmol) was added,Stir the mixture overnight.The reaction solution was concentrated on a column chromatography to give white solid 6 imidazo [1,2-a] pyridine-7-ol in 88% yield.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,33631-05-9, its application will become more common.

Reference:
Patent; East China Normal University; Hu Wenhao; Xi Jianbei; Lei Ruirui; Zhu Mengli; Ma Mingliang; Xiao Guolan; Zhang Xiongwen; Fang Yanfen; Li Hongyu; (28 pag.)CN106496222; (2017); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem