(1S,2R)-2-amino cyclopentanecarboxylic acid hydrochloride, with the CAS number 128052-92-6, 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 classification as an amino acid. The specific stereochemistry indicated by the (1S,2R) designation suggests that it has distinct spatial arrangements of its atoms, which 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 various chemical reactions, making it a versatile compound in organic synthesis and medicinal chemistry. Its unique structure and properties may also make it a candidate for studies related to peptide synthesis and drug development.

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

128052-92-6: (1S,2R)-2-amino cyclopentanecarboxylic acid hydrochloride, with the CAS number 128052-92-6, 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 classification as an amino acid. The specific stereochemistry indicated by the (1S,2R) designation suggests that it has distinct spatial arrangements of its atoms, which 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 various chemical reactions, making it a versatile compound in organic synthesis and medicinal chemistry. Its unique structure and properties may also make it a candidate for studies related to peptide synthesis and drug development.

CAS 128052-92-6

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

Cis-2-amino-cyclopentanecarboxylic acid hydrochloride

Ref: IN-DA000XPF

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

Ref: 7W-GM6867

(1S,2R)-2-aminocyclopentanecarboxylic acid hydrochloride

Ref: 54-OR308223