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CAS 149353-95-7

:

2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLINE-7-CARBOXYLIC ACID

Description:
2-(Tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-7-carboxylic acid is a chemical compound characterized by its complex structure, which includes a tetrahydroisoquinoline core, a carboxylic acid functional group, and a tert-butoxycarbonyl (Boc) protecting group. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules, due to its ability to undergo various chemical transformations. The presence of the Boc group allows for selective reactions while protecting the amine functionality, making it a valuable intermediate in peptide synthesis and other organic reactions. The compound is generally solid at room temperature and may exhibit solubility in organic solvents, depending on the specific conditions. Its reactivity is influenced by the functional groups present, allowing for further derivatization. As with many organic compounds, proper handling and storage are essential to maintain its stability and prevent degradation. Safety data sheets should be consulted for specific handling guidelines and potential hazards associated with this compound.
Formula:C15H19NO4
InChI:InChI=1/C15H19NO4/c1-15(2,3)20-14(19)16-7-6-10-4-5-11(13(17)18)8-12(10)9-16/h4-5,8H,6-7,9H2,1-3H3,(H,17,18)
SMILES:CC(C)(C)OC(=O)N1CCc2ccc(cc2C1)C(=O)O
Synonyms:
  • 3,4-Dihydro-1H-Isoquinoline-2,7-Dicarboxylic Acid 2-Tert-Butyl Ester
  • N-Boc-7-Hydroxycarbonyl-1,2,3,4-Tetrahydroisoquinoline
  • 2-[(Tert-Butoxy)Carbonyl]-1,2,3,4-Tetrahydroisoquinoline-7-Carboxylic Acid
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