6-Amino-2-N-Boc-1,2,3,4-tetrahydroisoquinoline

• CAT Number: R030307
• CAS Number: 164148-92-9
• Molecular Formula: C14H20N2O2
• Molecular Weight: 248.326
• Purity: ≥95%
• Synonyms: 6-Amino-2-(tert-butyloxycarbonyl)-1,2,3,4-tetrahydroisoquinoline; 6-Amino-2-N-Boc-1,2,3,4-tetrahydro-isoquinoline; 6-Amino-3,4-dihydro-2(1H)-isoquinolinecarboxylic Acid 1,1-Dimethylethyl Ester; 1,1-Dimethylethyl 6-amino-3,4-dihydro-2(1H)-isoquinoline
• Storage: -20°C
• IUPAC Name: tert-butyl 6-amino-3,4-dihydro-1H-isoquinoline-2-carboxylate
• InChI: InChI=1S/C14H20N2O2/c1-14(2,3)18-13(17)16-7-6-10-8-12(15)5-4-11(10)9-16/h4-5,8H,6-7,9,15H2,1-3H3
• InChIKey: OLOIFCYZWOTWRO-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)N1CCC2=C(C1)C=CC(=C2)N

6-Amino-2-N-Boc-1,2,3,4-tetrahydroisoquinoline is a protected tetrahydroisoquinoline derivative featuring a Boc (tert-butyloxycarbonyl) group attached to the nitrogen atom and an amino group at the 6-position. This compound is widely used in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. The Boc group protects the amine during reactions, allowing selective modifications of the molecule. Its structure makes it valuable in medicinal chemistry for developing therapeutic agents, including potential treatments for neurological and cardiovascular conditions.