(S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline

• CAT Number: R050660
• CAS Number: 118864-75-8
• Molecular Formula: C15H15N
• Molecular Weight: 209.29
• Purity: ≥95%
• Synonyms: (1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline; (+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline; (S)-(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
• Storage: -20°C
• IUPAC Name: (1S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline
• InChI: InChI=1S/C15H15N/c1-2-7-13(8-3-1)15-14-9-5-4-6-12(14)10-11-16-15/h1-9,15-16H,10-11H2/t15-/m0/s1
• InChIKey: PRTRSEDVLBBFJZ-HNNXBMFYSA-N
• SMILES: C1CNC(C2=CC=CC=C21)C3=CC=CC=C3

(S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline(CAT: R050660) is a chiral isoquinoline derivative featuring a phenyl group at the 1-position and a well-defined (S)-stereochemistry. This compound is widely utilized as a key intermediate in the synthesis of alkaloids, pharmaceutical candidates, and asymmetric catalysts. Its tetrahydroisoquinoline core mimics structural motifs found in biologically active molecules, particularly those affecting dopaminergic and serotonergic pathways. Due to its stereochemical integrity and pharmacophoric relevance, it is employed in enantioselective synthesis and medicinal chemistry for lead compound optimization.