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CAS 147228-37-3

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(R)-3-amino-5-phenyl-pentanoic acid-HCl

Description:
(R)-3-amino-5-phenyl-pentanoic acid-HCl, also known as a hydrochloride salt of a chiral amino acid, is characterized by its structural features that include an amino group, a carboxylic acid group, and a phenyl substituent on a pentanoic acid backbone. This compound exhibits properties typical of amino acids, such as the ability to form zwitterions at physiological pH, which contributes to its solubility in water. The presence of the phenyl group imparts hydrophobic characteristics, influencing its interactions in biological systems. As a hydrochloride salt, it is typically more stable and soluble than its free base form, making it suitable for pharmaceutical applications. The chiral nature of the molecule means it can exist in two enantiomeric forms, with the (R) configuration often being biologically active. This compound may be utilized in research related to neurochemistry or as a building block in peptide synthesis, given its structural similarity to naturally occurring amino acids.
Formula:C11H16ClNO2
InChI:InChI=1/C11H15NO2.ClH/c12-10(8-11(13)14)7-6-9-4-2-1-3-5-9;/h1-5,10H,6-8,12H2,(H,13,14);1H/t10-;/m1./s1
SMILES:c1ccc(cc1)CC[C@H](CC(=O)O)N.Cl
Synonyms:
  • (3R)-3-ammonio-5-phenylpentanoate
  • Benzenepentanoic acid, β-amino-, (betaR)-, hydrochloride (1:1)
  • H-D-β-Nva(5-phenyl)-OH.HCl
  • (R)-3-Amino-5-Phenylpentanoic Acid Hydrochloride
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