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CAS 132201-32-2

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Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride (1:1), (αR,βS)-

Description:
Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride (1:1), (αR,βS)- is a chemical compound characterized by its structural features that include a benzene ring, a propanoic acid moiety, and both amino and hydroxy functional groups. This compound is typically classified as an amino acid derivative, exhibiting properties such as solubility in water due to the presence of the hydrochloride form, which enhances its ionic character. The specific stereochemistry indicated by (αR,βS) suggests that it has defined spatial arrangements of its atoms, which can influence its biological activity and interactions. As a hydrochloride salt, it is likely to be more stable and easier to handle than its free base form. This compound may have applications in pharmaceuticals or biochemistry, particularly in studies related to amino acid metabolism or as a potential therapeutic agent. Its CAS number, 132201-32-2, allows for precise identification and reference in scientific literature and databases.
Formula:C9H11NO3·ClH
InChI:InChI=1S/C9H11NO3.ClH/c10-7(8(11)9(12)13)6-4-2-1-3-5-6;/h1-5,7-8,11H,10H2,(H,12,13);1H/t7-,8+;/m0./s1
InChI key:InChIKey=OTJZSGZNPDLQAJ-KZYPOYLOSA-N
SMILES:[C@H]([C@H](C(O)=O)O)(N)C1=CC=CC=C1.Cl
Synonyms:
  • (1S,2R)-2-carboxy-2-hydroxy-1-phenylethanaminium chloride
  • (2R,3S)-3-Amino-2-Hydroxy-3-Phenyl-Propanoic Acid Hydrochloride
  • (2R,3S)-3-Amino-2-hydroxy-3-phenyl-propanoic acid
  • (2R,3S)-3-Amino-2-hydroxy-3-phenylpropanic acid
  • (2R,3S)-3-Phenylisoserine hydrochloride
  • (2R,3S)-3-ammonio-2-hydroxy-3-phenylpropanoate
  • (2R,3S)-Phenylisoserine Hydrochloride
  • 3-(2R,3S)-Phenylisoserine
  • Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride (1:1), (αR,βS)-
  • Benzenepropanoic acid, β-amino-α-hydroxy-, hydrochloride, (αR,βS)-
  • See more synonyms
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