Benzimidazole

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Identification

Molecular formula
C13H12N4
CAS Number
41859-89-8
IUPAC Name
2-[(6-carbamimidoyl-1H-benzimidazol-2-yl)methyl]-3H-benzimidazole-5-carboxamidine
Molecular Weight
209.26g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3700g/cm3
Synonyms
BABIM
Interesting facts

Interesting Facts about 2-[(6-carbamimidoyl-1H-benzimidazol-2-yl)methyl]-3H-benzimidazole-5-carboxamidine

This intriguing compound, known as 2-[(6-carbamimidoyl-1H-benzimidazol-2-yl)methyl]-3H-benzimidazole-5-carboxamidine, belongs to the class of compounds that feature benzimidazole, a structure well known for its various biological activities. Here are some captivating aspects of this compound:

  • Biological Significance: Benzimidazole derivatives have gained considerable attention in medicinal chemistry due to their diverse biological properties, including antimicrobial, anti-inflammatory, and anticancer activities.
  • Structure-Activity Relationship: The substitution pattern on the benzene rings in this compound can significantly affect its pharmacological properties, making it a subject of study for drug design. The presence of the carboxamidine functional group is particularly noteworthy, as it can enhance the biological activity and solubility of the compound.
  • Potential Applications: Compounds with similar structures have been explored for use in treating various diseases, including infections, cancer, and neurological disorders. Thus, understanding the effects of this specific compound might lead to advancements in therapeutic options.
  • Research Opportunities: This compound’s unique molecular design provides a rich field for further investigation. Scientists could explore its mechanism of action, efficacy, and safety profiles through both in vitro and in vivo studies.
  • Synthesis Challenges: The intricate synthesis of such compounds can present challenges due to the need for precise control over reaction conditions. Mastery of organic synthesis techniques is crucial for chemists working with such derivatives.

In essence, 2-[(6-carbamimidoyl-1H-benzimidazol-2-yl)methyl]-3H-benzimidazole-5-carboxamidine represents a promising avenue for scientific exploration that bridges the gaps between chemistry and therapeutic development. As research continues, it may reveal even more mysteries and applications that could significantly impact the field of medicinal chemistry.

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