(1S,2R)-(+)-Chloroephedrine is a chiral compound that belongs to the class of phenethylamines, specifically a derivative of ephedrine. It features a chlorinated structure, which contributes to its unique pharmacological properties. This substance is characterized by its stereochemistry, with specific configurations at the first and second carbon atoms, which influence its biological activity and interaction with receptors. (1S,2R)-(+)-Chloroephedrine is known for its sympathomimetic effects, making it relevant in medicinal chemistry, particularly in the development of drugs for respiratory conditions. Its solubility profile typically indicates moderate solubility in polar solvents, and it may exhibit varying degrees of stability under different environmental conditions. The compound's potential applications in pharmaceuticals are often explored in the context of its efficacy and safety, as well as its role in the synthesis of other bioactive molecules. As with many chiral compounds, the specific enantiomer can have significantly different effects, underscoring the importance of stereochemistry in drug design and therapeutic use.

(1S,2R)-(+)-chloroephedrine

1384199-95-4: (1S,2R)-(+)-Chloroephedrine is a chiral compound that belongs to the class of phenethylamines, specifically a derivative of ephedrine. It features a chlorinated structure, which contributes to its unique pharmacological properties. This substance is characterized by its stereochemistry, with specific configurations at the first and second carbon atoms, which influence its biological activity and interaction with receptors. (1S,2R)-(+)-Chloroephedrine is known for its sympathomimetic effects, making it relevant in medicinal chemistry, particularly in the development of drugs for respiratory conditions. Its solubility profile typically indicates moderate solubility in polar solvents, and it may exhibit varying degrees of stability under different environmental conditions. The compound's potential applications in pharmaceuticals are often explored in the context of its efficacy and safety, as well as its role in the synthesis of other bioactive molecules. As with many chiral compounds, the specific enantiomer can have significantly different effects, underscoring the importance of stereochemistry in drug design and therapeutic use.

CAS 1384199-95-4

(1S,2R)-(+)-chloroephedrine

Ephedrine Impurity 15 HCl

Ref: 4Z-E-128027