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CS-W001157 4
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1H-Benzo[d]imidazol-6-amine

  • CAS No. 934-22-5

  • Cat. No. CS-0096864
  • Purity≥97%
  • MDL No.MFCD00465258

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

1H-Benzo[d]imidazol-6-amine|CS-0096864

Structure of 934-22-5

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General Information

  • CAS No. 934-22-5
  • Cat. No. CS-0096864
  • Purity ≥97%
  • MDL No. MFCD00465258
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₇N₃
  • Molecular Weight 133.15
  • Synonym(s) 5-Aminobenzimidazole
  • SMILES NC1=CC=C2N=CNC2=C1

Description

1H-Benzo[d]imidazol-6-amine features a fused bicyclic core with a primary amine at the 6-position, enabling direct functionalization in medicinal chemistry. This electron-rich heterocycle exhibits enhanced solubility and stability under standard conditions, facilitating its use in scaffold diversification and bioactive molecule synthesis.

Synthesis

  • Route1

    References

    • CYTOPIA RESEARCH PTY LTD Patent: WO2005/66156 A1, 2005 ; Location in patent: Page/Page column 33 ; WO 2005/066156 A1
  • Route2
    • null|null
      64-18-6
    • Benzene-1,2,4-triamine|CS-0737175
      615-71-4
    • ~81%
    • In-stock
      1H-Benzo[d]imidazol-6-amine|CS-0096864
      934-22-5

    References

    • Karuvalam, Ranjith P.; Haridas, Karickal R.; Shetty, Suchetha N. Journal of the Chilean Chemical Society, 2012 , vol. 57, # 2 p. 1122 - 1125,4
  • Route3
    • null|null
      64-18-6
    • ~%
    • In-stock
      1H-Benzo[d]imidazol-6-amine|CS-0096864
      934-22-5

    References

    • Recueil des Travaux Chimiques des Pays-Bas, , vol. 67, p. 45,48,51 Helvetica Chimica Acta, , vol. 32, p. 135,143,144 Journal of Biological Chemistry, , vol. 152, p. 225,227

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-H319
Precautionary Statements : P264-P270-P280

Quality Control

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Computational Chemistry Data

  • TPSA   54.7
  • LogP   1.1451
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   0

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