Date published: 2025-9-25

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2-(2-Aminophenyl)-1H-benzimidazole (CAS 5805-39-0)

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CAS Number:
5805-39-0
Purity:
98%
Molecular Weight:
209.25
Molecular Formula:
C13H11N3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-(2-Aminophenyl)-1H-benzimidazole is frequently used in the field of chemistry and biochemistry for its role as a building block in the synthesis of more complex organic compounds. Its unique structure, which features both a benzimidazole and an aminophenyl group, allows it to interact with various biological targets, providing insights into molecular recognition processes. Research involving 2-(2-Aminophenyl)-1H-benzimidazole often focuses on exploring its binding properties with DNA and proteins, which is for understanding cellular mechanisms and designing novel compounds with specific biological activities. Moreover, this chemical is instrumental in the study of fluorescence properties in biological systems, as its structure can be modified to emit fluorescence under certain conditions.


2-(2-Aminophenyl)-1H-benzimidazole (CAS 5805-39-0) References

  1. Design, selection, and characterization of thioflavin-based intercalation compounds with metal chelating properties for application in Alzheimer's disease.  |  Rodríguez-Rodríguez, C., et al. 2009. J Am Chem Soc. 131: 1436-51. PMID: 19133767
  2. Microwave synthesis, crystal structure, antioxidant, and antimicrobial study of new 6-heptyl-5,6-dihydrobenzo[4,5]imidazo[1,2-c]quinazoline compound.  |  Hasan, HA., et al. 2018. Chem Cent J. 12: 145. PMID: 30570683
  3. Novel ion imprinted polymer electrochemical sensor for the selective detection of lead(II).  |  Dahaghin, Z., et al. 2020. Food Chem. 303: 125374. PMID: 31473457
  4. Inhibition of albendazole and 2-(2-aminophenyl)-1H-benzimidazole against tyrosinase: mechanism, structure-activity relationship, and anti-browning effect.  |  Wen, Y., et al. 2023. J Sci Food Agric. 103: 2824-2837. PMID: 36641547
  5. Synthesis, structural diversity and luminescent properties of cadmium (II) coordination assemblies with 2-(2-aminophenyl)-1H-benzimidazole and pseudohalide ions.  |  Nawrot, I., Czerwińska, K., Machura, B., & Kruszynski, R. 2017. Journal of Luminescence. 181: 103-113.
  6. A zinc (II) metal–organic complex based on 2-(2-aminophenyl)-1H-benzimidazole ligand: Exhibiting high adsorption capacity for aromatic hazardous dyes and catecholase mimicking activity  |  Muslim, M., Ali, A., Ahmad, M., Alarifi, A., Afzal, M., Sepay, N., & Dege, N. 2022. Journal of Molecular Liquids. 363: 119767.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-(2-Aminophenyl)-1H-benzimidazole, 5 g

sc-229846
5 g
$43.00