The chemical substance known as (S)-1-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine maleic acid is a complex organic compound characterized by its chiral centers and functional groups. It features a phenylbutenamine backbone, which contributes to its potential biological activity, particularly in medicinal chemistry. The presence of trifluoromethyl groups enhances lipophilicity and may influence the compound's pharmacokinetic properties. The maleic acid moiety suggests the potential for forming salts or complexes, which can affect solubility and stability. This compound's stereochemistry is crucial for its interaction with biological targets, as the (S) and (R) configurations can significantly alter its efficacy and safety profile. Overall, this substance may exhibit interesting properties for research in drug development, particularly in areas requiring selective activity against specific biological pathways. However, detailed studies would be necessary to fully understand its behavior and applications in various chemical and biological contexts.

(S)-1-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine maleic acid

1214741-14-6: The chemical substance known as (S)-1-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine maleic acid is a complex organic compound characterized by its chiral centers and functional groups. It features a phenylbutenamine backbone, which contributes to its potential biological activity, particularly in medicinal chemistry. The presence of trifluoromethyl groups enhances lipophilicity and may influence the compound's pharmacokinetic properties. The maleic acid moiety suggests the potential for forming salts or complexes, which can affect solubility and stability. This compound's stereochemistry is crucial for its interaction with biological targets, as the (S) and (R) configurations can significantly alter its efficacy and safety profile. Overall, this substance may exhibit interesting properties for research in drug development, particularly in areas requiring selective activity against specific biological pathways. However, detailed studies would be necessary to fully understand its behavior and applications in various chemical and biological contexts.

CAS 1214741-14-6

(S)-1-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-2-phenylbut-3-en-2-amine maleic acid

Benzenemethanamine, α-[[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy]methyl]-α-ethenyl-, (αS)-, (2Z)-2-butenedioate (1:1)

Ref: IN-DA00150M