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CAS 270065-70-8

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(S)-3-amino-4-(4-iodo-phenyl)-butyric acid-HCl

Description:
(S)-3-amino-4-(4-iodo-phenyl)-butyric acid-HCl, with the CAS number 270065-70-8, is a chiral amino acid derivative characterized by its specific stereochemistry and functional groups. This compound features an amino group (-NH2), a carboxylic acid group (-COOH), and a phenyl ring substituted with an iodine atom, contributing to its unique properties. The presence of the hydrochloride (HCl) salt form indicates that it is likely soluble in water, enhancing its bioavailability for potential pharmaceutical applications. The iodo substitution on the phenyl ring can influence the compound's reactivity and biological activity, making it of interest in medicinal chemistry. As a chiral molecule, it may exhibit different pharmacological effects depending on its stereoisomer, which is crucial in drug development. Overall, this compound's structure suggests potential uses in research and therapeutic contexts, particularly in areas related to neurochemistry or as a building block for more complex molecules.
Formula:C10H12INO2
InChI:InChI=1/C10H12INO2.ClH/c11-8-3-1-7(2-4-8)5-9(12)6-10(13)14;/h1-4,9H,5-6,12H2,(H,13,14);1H/t9-;/m0./s1
SMILES:c1cc(ccc1C[C@@H](CC(=O)O)N)I.Cl
Synonyms:
  • L-3-Amino-4-(4-iodophenyl)-butyric acid Hydrochloride
  • (3S)-3-amino-4-(4-iodophenyl)butanoic acid hydrochloride
  • H-β-HoPhe(4-I)-OH.HCl
  • (S)-3-Amino-4-(4-Iodophenyl)Butanoic Acid Hydrochloride
  • S-3-Amino-4-(4-iodo-phenyl)butyric acid
  • H-PHE(4-I)-(C*CH2)OH HCL
  • 4-IODO-L-BETA-HOMOPHENYLALANINE HYDROCHLORIDE
  • (S)-3-AMINO-4-(4-IODO-PHENYL)-BUTYRIC ACID HCL
  • (S)-b-Amino-4-iodobenzenebutanoic acid
  • H-BETA-HOPHE(4-I)-OH HCL
  • See more synonyms
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