Cyclopropaneacetic acid, a-[[1S)-1-phenylethyl]amino]-, (aS)- is a chemical compound characterized by its unique structure, which includes a cyclopropane ring and an acetic acid moiety. This compound features an amino group attached to a chiral center, contributing to its stereochemistry. The presence of the phenylethyl group enhances its potential for interactions in biological systems, making it of interest in medicinal chemistry. The cyclopropane ring introduces strain, which can influence the reactivity and stability of the molecule. Typically, compounds like this may exhibit specific solubility properties, depending on the functional groups present, and may participate in various chemical reactions such as acylation or amination. The stereochemistry indicated by the (aS)- designation suggests that the compound can exist in different enantiomeric forms, which can have significant implications for its biological activity and pharmacological properties. Overall, this compound's unique structural features make it a subject of interest for further research in organic synthesis and drug development.

Cyclopropaneaceticacid, a-[[(1S)-1-phenylethyl]amino]-, (aS)-

281191-43-3: Cyclopropaneacetic acid, a-[[1S)-1-phenylethyl]amino]-, (aS)- is a chemical compound characterized by its unique structure, which includes a cyclopropane ring and an acetic acid moiety. This compound features an amino group attached to a chiral center, contributing to its stereochemistry. The presence of the phenylethyl group enhances its potential for interactions in biological systems, making it of interest in medicinal chemistry. The cyclopropane ring introduces strain, which can influence the reactivity and stability of the molecule. Typically, compounds like this may exhibit specific solubility properties, depending on the functional groups present, and may participate in various chemical reactions such as acylation or amination. The stereochemistry indicated by the (aS)- designation suggests that the compound can exist in different enantiomeric forms, which can have significant implications for its biological activity and pharmacological properties. Overall, this compound's unique structural features make it a subject of interest for further research in organic synthesis and drug development.

CAS 281191-43-3

Cyclopropaneaceticacid, a-[[(1S)-1-phenylethyl]amino]-, (aS)-

(2S,1''S)-2-CYCLOPROPYL-2-(1-PHENYLETHYLAMINO)ACETIC ACID

Ref: IN-DA00BDGF