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2-Bromo-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole

  • CAS No. 1525619-20-8

  • Cat. No. CS-0145130
  • Purity≥97%
  • MDL No.MFCD29047774

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

2-Bromo-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole|CS-0145130

Structure of 1525619-20-8

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General Information

  • CAS No. 1525619-20-8
  • Cat. No. CS-0145130
  • Purity ≥97%
  • MDL No. MFCD29047774
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₇BrN₂
  • Molecular Weight 187.04
  • Synonym(s) 2-Bromo-5H,6H,7H-pyrrolo[1,2-A]imidazole
  • SMILES BrC1=CN2C(CCC2)=N1

Description

2-Bromo-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole is a heterocyclic scaffold featuring a brominated imidazole core with enhanced stability and tunable reactivity. This bench-stable compound integrates readily into transition-metal-catalyzed coupling reactions, enabling efficient access to functionalized pyrroloimidazoles for medicinal chemistry applications.

Application

2-Bromo-6,7-dihydro-5H-pyrrolo[1,2-a]imidazole serves as a versatile building block for the synthesis of functionalized purine analogs and heterocyclic scaffolds. The bromine substituent enables palladium-catalyzed cross-coupling reactions, facilitating C–C bond formation under mild conditions. Its saturated imidazole core provides enhanced stability and solubility compared to aromatic counterparts, while maintaining compatibility with standard protecting group strategies. This compound functions effectively in late-stage diversification workflows common in medicinal chemistry.

Safety Information

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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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   17.82
  • LogP   1.5918
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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