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5-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride

  • CAS No. 1197595-75-7

  • Cat. No. CS-0101638
  • Purity≥97%
  • MDL No.MFCD12761523

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

5-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride|CS-0101638

Structure of 1197595-75-7

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General Information

  • CAS No. 1197595-75-7
  • Cat. No. CS-0101638
  • Purity ≥97%
  • MDL No. MFCD12761523
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₁BrClN
  • Molecular Weight 248.55
  • Synonym(s) 5-BROMO-2,3-DIHYDRO-1H-INDEN-1-AMINE-HCl
  • SMILES NC1CCC2=C1C=CC(Br)=C2.[H]Cl

Description

This bench-stable indenamine derivative features a brominated aromatic core and a protonated amine, enabling straightforward incorporation into transition metal-catalyzed cross-coupling reactions. The hydrochloride salt enhances solubility in polar solvents, facilitating use in synthetic workflows requiring precise nitrogen delivery.

Application

5-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride serves as a versatile building block in medicinal chemistry, enabling efficient access to indoline scaffolds via palladium-catalyzed cross-coupling and electrophilic functionalization. The bromo group facilitates C–C and C–N bond formation under standard conditions, while the amine functionality provides a handle for derivatization and salt formation. Its bench-stable crystalline form supports straightforward handling and purification, making it well-suited for iterative synthesis workflows and API intermediate development.

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   26.02
  • LogP   2.8169
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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