(αS,βS)-β-[(2-Aminophenyl)thio]-α-hydroxy-4-methoxybenzenepropanoic Acid Methyl Ester

• CAT Number: R053118
• CAS Number: 99109-07-6
• Molecular Formula: C17H19NO4S
• Molecular Weight: 333.402
• Purity: ≥95%
• Synonyms: [S-(R*,R*)]-β-[(2-Aminophenyl)thio]-α-hydroxy-4-methoxybenzenepropanoic Acid Methyl Ester
• Storage: -20°C
• IUPAC Name: methyl (2S,3S)-3-(2-aminophenyl)sulfanyl-2-hydroxy-3-(4-methoxyphenyl)propanoate
• InChI: InChI=1S/C17H19NO4S/c1-21-12-9-7-11(8-10-12)16(15(19)17(20)22-2)23-14-6-4-3-5-13(14)18/h3-10,15-16,19H,18H2,1-2H3/t15-,16+/m1/s1
• InChIKey: MPWGGMIUPWSNEV-CVEARBPZSA-N
• SMILES: COC1=CC=C(C=C1)C(C(C(=O)OC)O)SC2=CC=CC=C2N

(αS,βS)-β-[(2-Aminophenyl)thio]-α-hydroxy-4-methoxybenzenepropanoic Acid Methyl Ester is a complex organic compound used primarily in advanced synthetic chemistry and pharmaceutical research. The molecule features a thioether bond, an aminophenyl group, and a hydroxy group, giving it diverse reactivity and potential biological activity. Its stereochemistry, with specific (αS,βS) configuration, plays a crucial role in its interactions with biological targets, making it a key intermediate for the synthesis of chiral molecules. The compound is often involved in the development of novel drugs, particularly those aimed at modulating enzyme activity or receptor binding, making it valuable for medicinal chemistry and biochemical research.