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CS-W001157 4
Total: USD 88.00

1-Boc-6-Amino-2,3-dihydroindole

  • CAS No. 129488-00-2

  • Cat. No. CS-M1316
  • Purity≥98%
  • MDL No.MFCD08059271

*For research and further manufacturing use only, not for direct human use.

1-Boc-6-Amino-2,3-dihydroindole|CS-M1316

Structure of 129488-00-2

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General Information

  • CAS No. 129488-00-2
  • Cat. No. CS-M1316
  • Purity ≥98%
  • MDL No. MFCD08059271
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₁₈N₂O₂
  • Molecular Weight 234.30
  • Synonym(s) tert-Butyl 6-aminoindoline-1-carboxylate
  • SMILES O=C(OC(C)(C)C)N1C2=CC(N)=CC=C2CC1

Description

1-Boc-6-Amino-2,3-dihydroindole is a bench-stable, moisture-tolerant building block featuring a protected primary amine and electron-rich dihydroindole core. This functionalized scaffold integrates seamlessly into synthetic routes for indole-based pharmaceuticals and bioactive heterocycles, enabling straightforward deprotection and further derivatization under standard conditions.

Application

1-Boc-6-Amino-2,3-dihydroindole serves as a versatile building block for the synthesis of indole-based scaffolds in medicinal chemistry and natural product synthesis. The Boc group provides stability and ease of deprotection under mild acidic conditions, while the pendant amine enables further functionalization via coupling reactions. Its compatibility with standard synthetic protocols makes it valuable for constructing complex heterocycles and peptide-like architectures.

Synthesis

  • Route1

    References

    • Carruthers, Nicholas I.; Chai, Wenying; Dax, Scott L.; Jablonowski, Jill A.; Li, Xiaobing; Lovenberg, Timothy W.; Murray, William V.; Rudolph, Dale A.; Seierstad, Mark; Youngman, Mark A. Patent: US2005/70534 A1, 2005 ; Location in patent: Page/Page column 11 ; US 20050070534 A1
  • Route2
    • tert-Butyl 6-nitro-1H-indole-1-carboxylate|CS-M1315
      219552-64-4
    • ~88%
    • In-stock
      1-Boc-6-Amino-2,3-dihydroindole|CS-M1316
      129488-00-2

    References

    • Varnes, Jeffrey G.; Wacker, Dean A.; Jacobson, Irina C.; Quan, Mimi L.; Ellis, Christopher D.; Rossi, Karen A.; He, Ming Y.; Luettgen, Joseph M.; Knabb, Robert M.; Bai, Steven; He, Kan; Lam, Patrick Y.S.; Wexler, Ruth R. Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 23 p. 6481 - 6488
  • Route3
    • null|null
      545393-63-3
    • ~%
    • In-stock
      1-Boc-6-Amino-2,3-dihydroindole|CS-M1316
      129488-00-2

    References

    • US2003/195201 A1, ; US 20030195201 A1

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   55.56
  • LogP   2.5664
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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