Ethanol, 2-[[[4S]-4-[(7-chloro-4-quinolinyl)amino]pentyl]ethylamino]-, phosphate (salt), with CAS number 645406-45-7, is a chemical compound that features a complex structure incorporating both an ethanol moiety and a phosphate group. This compound is characterized by its potential biological activity, particularly in pharmaceutical applications, due to the presence of the quinoline and amino groups, which may contribute to its interaction with biological targets. The chloro substituent on the quinoline ring enhances its pharmacological properties, potentially influencing its efficacy and selectivity. As a salt, it may exhibit improved solubility and stability compared to its free base form, making it more suitable for formulation in various applications. The compound's stereochemistry, indicated by the (4S) designation, suggests specific spatial arrangements that can significantly affect its biological interactions. Overall, this compound is of interest in medicinal chemistry, particularly in the development of therapeutic agents.

Ethanol, 2-[[(4S)-4-[(7-chloro-4-quinolinyl)amino]pentyl]ethylamino]-,phosphate (salt)

645406-45-7: Ethanol, 2-[[[4S]-4-[(7-chloro-4-quinolinyl)amino]pentyl]ethylamino]-, phosphate (salt), with CAS number 645406-45-7, is a chemical compound that features a complex structure incorporating both an ethanol moiety and a phosphate group. This compound is characterized by its potential biological activity, particularly in pharmaceutical applications, due to the presence of the quinoline and amino groups, which may contribute to its interaction with biological targets. The chloro substituent on the quinoline ring enhances its pharmacological properties, potentially influencing its efficacy and selectivity. As a salt, it may exhibit improved solubility and stability compared to its free base form, making it more suitable for formulation in various applications. The compound's stereochemistry, indicated by the (4S) designation, suggests specific spatial arrangements that can significantly affect its biological interactions. Overall, this compound is of interest in medicinal chemistry, particularly in the development of therapeutic agents.

CAS 645406-45-7

Ethanol, 2-[[(4S)-4-[(7-chloro-4-quinolinyl)amino]pentyl]ethylamino]-,phosphate (salt)

(S)-(+)-Hydroxy Chloroquine-d4 Diphosphate

Ref: TR-H905307