(1R,2S)-2-amino cyclopentanecarboxylic acid hydrochloride, with the CAS number 128110-37-2, is a chiral amino acid derivative characterized by its cyclopentane ring structure. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH) attached to the cyclopentane, which contributes to its properties as an amino acid. The specific stereochemistry indicated by the (1R,2S) configuration suggests that it has distinct spatial arrangements that can influence its biological activity and interactions. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in various applications, including pharmaceuticals and biochemical research. The presence of the amino and carboxylic acid functional groups allows it to participate in typical amino acid reactions, such as peptide bond formation. Its unique structure and properties make it of interest in studies related to protein synthesis and drug development, particularly in the context of chirality and its effects on biological systems.

(1R,2S)-2-amino cyclopetanecarboxylic acid hydrochloride

128110-37-2: (1R,2S)-2-amino cyclopentanecarboxylic acid hydrochloride, with the CAS number 128110-37-2, is a chiral amino acid derivative characterized by its cyclopentane ring structure. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH) attached to the cyclopentane, which contributes to its properties as an amino acid. The specific stereochemistry indicated by the (1R,2S) configuration suggests that it has distinct spatial arrangements that can influence its biological activity and interactions. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in various applications, including pharmaceuticals and biochemical research. The presence of the amino and carboxylic acid functional groups allows it to participate in typical amino acid reactions, such as peptide bond formation. Its unique structure and properties make it of interest in studies related to protein synthesis and drug development, particularly in the context of chirality and its effects on biological systems.

CAS 128110-37-2

(1R,2S)-2-amino cyclopetanecarboxylic acid hydrochloride

(1R,2S)-(-)-2-Amino-1-cyclopentanecarboxylic acid hydrochloride

Ref: IN-DA000XT3

(1R,2S)-(-)-2-Amino-1-cyclopentanecarboxylic acid hydrochloride hemihydrate

Ref: 7W-GM1898

(1R,2S)-2-Amino-cyclopentanecarboxylic acid hydrochloride

Ref: 54-OR307663

(1R,2S)-2-Aminocyclopentane-1-carboxylic acid hydrochloride

Ref: 10-F620381