2-Chloro-5,6,7,8-tetrahydroquinolin-8-ol is a chemical compound characterized by its unique bicyclic structure, which consists of a quinoline core with a hydroxyl group and a chlorine substituent. This compound features a tetrahydroquinoline framework, indicating that it has undergone partial hydrogenation, resulting in a saturated ring system. The presence of the hydroxyl (-OH) group contributes to its potential as a phenolic compound, influencing its solubility and reactivity. The chlorine atom introduces additional reactivity and can affect the compound's biological activity. Typically, compounds of this nature may exhibit various pharmacological properties, making them of interest in medicinal chemistry. The molecular structure allows for potential interactions with biological targets, which could lead to applications in drug development. Additionally, the compound's stability, solubility in organic solvents, and reactivity with nucleophiles or electrophiles are important characteristics that define its behavior in chemical reactions and potential uses in synthesis or as a therapeutic agent.

2-chloro-5,6,7,8-tetrahydroquinolin-8-ol

130861-73-3: 2-Chloro-5,6,7,8-tetrahydroquinolin-8-ol is a chemical compound characterized by its unique bicyclic structure, which consists of a quinoline core with a hydroxyl group and a chlorine substituent. This compound features a tetrahydroquinoline framework, indicating that it has undergone partial hydrogenation, resulting in a saturated ring system. The presence of the hydroxyl (-OH) group contributes to its potential as a phenolic compound, influencing its solubility and reactivity. The chlorine atom introduces additional reactivity and can affect the compound's biological activity. Typically, compounds of this nature may exhibit various pharmacological properties, making them of interest in medicinal chemistry. The molecular structure allows for potential interactions with biological targets, which could lead to applications in drug development. Additionally, the compound's stability, solubility in organic solvents, and reactivity with nucleophiles or electrophiles are important characteristics that define its behavior in chemical reactions and potential uses in synthesis or as a therapeutic agent.

CAS 130861-73-3

2-chloro-5,6,7,8-tetrahydroquinolin-8-ol

2-Chloro-5,6,7,8-tetrahydroquinolin-8-ol

Ref: 54-OR1002453

2-Chloro-5,6,7,8-tetrahydroquinolin-8-ol

Ref: 10-F783860