Date published: 2026-5-17

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2,2′-Biimidazole (CAS 492-98-8)

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CAS Number:
492-98-8
Purity:
≥98%
Molecular Weight:
134.14
Molecular Formula:
C6H6N4
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
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′-Biimidazole is a white powder and demonstrates solubility in polar solvents like methanol, water, and dimethyl sulfoxide (DMSO). This compound acts as a Lewis base, capable of coordinating with metal ions such as Cu(I), Ag(I), and Au(I-II). The resultant coordination compounds have exhibited catalytic activity superior to other metal-ligand complexes. 2,2′-Biimidazole is used as a building block in the construction of supramolecular structures, nanoparticles, and other coordination compounds. Its role as a ligand in catalysis contributes to enhanced efficiency in chemical reactions. Additionally, 2,2′-Biimidazole has also been used in the synthesis of fluorescent proteins, facilitating the exploration of protein structure and function within cells.


2,2′-Biimidazole (CAS 492-98-8) References

  1. Bis[2-(1H-imidazol-2-yl-κN)-1H-imidazol-3-ium]silver(I) trinitrate.  |  Finch, SR., et al. 2011. Acta Crystallogr Sect E Struct Rep Online. 67: m909. PMID: 21836895
  2. A Comprehensive Study on the Dye Adsorption Behavior of Polyoxometalate-Complex Nano-Hybrids Containing Classic β-Octamolybdate and Biimidazole Units.  |  Liang, S., et al. 2019. Molecules. 24: PMID: 30813387
  3. Inhibition of autophagic flux by cyclometalated iridium(iii) complexes through anion transportation.  |  Chen, MH., et al. 2019. Chem Sci. 10: 3315-3323. PMID: 30996918
  4. Similarities and differences in d6 low-spin ruthenium, rhodium and iridium half-sandwich complexes: synthesis, structure, cytotoxicity and interaction with biological targets.  |  Gilewska, A., et al. 2019. J Biol Inorg Chem. 24: 591-606. PMID: 31115765
  5. Cross-Electrophile Coupling of Unactivated Alkyl Chlorides.  |  Sakai, HA., et al. 2020. J Am Chem Soc. 142: 11691-11697. PMID: 32564602
  6. Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagent.  |  Uchikura, T., et al. 2020. Beilstein J Org Chem. 16: 2442-2447. PMID: 33082878
  7. Phosphorescent metal complexes as theranostic anticancer agents: combining imaging and therapy in a single molecule.  |  Tan, CP., et al. 2021. Chem Sci. 12: 2357-2367. PMID: 34164000
  8. Interaction of a 1,3-Dicarbonyl Toxin with Ru(II)-Biimidazole Complexes for Luminescence Sensing: A Spectroscopic and Photochemical Experimental Study Rationalized by Time-Dependent Density Functional Theory Calculations.  |  Quílez-Alburquerque, J., et al. 2022. Inorg Chem. 61: 328-337. PMID: 34923820
  9. Insights on the Synthesis of N-Heterocycles Containing Macrocycles and Their Complexion and Biological Properties.  |  Malek, F., et al. 2022. Molecules. 27: PMID: 35408522
  10. Unexpected molecular diversity of brown carbon formed by Maillard-like reactions in aqueous aerosols.  |  Tang, S., et al. 2022. Chem Sci. 13: 8401-8411. PMID: 35919720
  11. RUNAT-BI: A Ruthenium(III) Complex as a Selective Anti-Tumor Drug Candidate against Highly Aggressive Cancer Cell Lines.  |  Albanell-Fernández, M., et al. 2022. Cancers (Basel). 15: PMID: 36612065
  12. Bipyridine Ruthenium(II) Complexes with Halogen-Substituted Salicylates: Synthesis, Crystal Structure, and Biological Activity.  |  Schoeller, M., et al. 2023. Molecules. 28: PMID: 37375164
  13. Recent advances in fluorescent materials for mercury(ii) ion detection.  |  Li, Q. and Zhou, Y. 2023. RSC Adv. 13: 19429-19446. PMID: 37383685

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,2′-Biimidazole, 1 g

sc-298557
1 g
$84.00

2,2′-Biimidazole, 5 g

sc-298557A
5 g
$388.00