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Benzimidazole-5-carboximidamide

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Identification
Molecular formula
C8H9N3
CAS number
7472-26-6
IUPAC name
3H-benzimidazole-5-carboxamidine
State
State

At room temperature, benzimidazole-5-carboximidamide exists as a solid. This is typical for many small, heterocyclic organic compounds, as they generally possess a crystalline lattice that contributes to their stability in the solid state.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.00
Boiling point (Celsius)
365.00
Boiling point (Kelvin)
638.00
General information
Molecular weight
161.18g/mol
Molar mass
161.1840g/mol
Density
1.3000g/cm3
Appearence

Benzimidazole-5-carboximidamide typically appears as a crystalline solid. The crystals are often colorless or white, depending on the purity and specific conditions of synthesis. Given the structure of the compound, it might also show distinct spectral properties when analyzed using spectroscopic methods.

Comment on solubility

Solubility of 3H-benzimidazole-5-carboxamidine (C8H9N3)

The solubility of 3H-benzimidazole-5-carboxamidine is an important aspect to consider, particularly in the context of its potential applications in various fields such as pharmaceuticals. The compound demonstrates variable solubility depending on several factors, which are summarized as follows:

  • Solvent Polarity: 3H-benzimidazole-5-carboxamidine tends to be soluble in polar solvents due to its functional groups.
  • pH Levels: The solubility can be significantly affected by the acidity or basicity of the solution, suggesting that it may be more soluble in acidic conditions.
  • Temperature: Increasing the temperature generally enhances solubility for many solid compounds, including this one.
  • Concentration: At higher concentrations, there might be limited solubility, leading to possible precipitation.

To illustrate its potential behavior, one might note that "solubility is not merely a characteristic of a compound but a dynamic interaction involving molecular forces." Thus, understanding the solubility of 3H-benzimidazole-5-carboxamidine leads to insights not only into its properties but also into its reactivity and functionality in diverse chemical environments.

In conclusion, while 3H-benzimidazole-5-carboxamidine exhibits promising solubility characteristics, further experimental investigation is essential to quantify these properties under various conditions. This will aid in unlocking its full potential in practical applications.

Interesting facts

Interesting Facts about 3H-benzimidazole-5-carboxamidine

3H-benzimidazole-5-carboxamidine is a fascinating compound that belongs to the family of benzimidazole derivatives, which have garnered significant attention in the fields of medicinal and organic chemistry. Here are some notable aspects of this intriguing compound:

  • Biological Importance: Benzimidazole derivatives, including 3H-benzimidazole-5-carboxamidine, are often recognized for their biological activities. They exhibit a variety of *pharmacological properties*, making them potential candidates in drug development.
  • Mechanism of Action: This compound can function as an inhibitor of specific enzymes and may play a role in *mitochondrial function*. Its interactions with biological targets can lead to therapeutic applications, particularly in treating diseases such as cancer and fungal infections.
  • Synthetic Versatility: The synthesis of 3H-benzimidazole-5-carboxamidine can be achieved through various methods, making it a *valuable intermediate* in organic synthesis. Its structural characteristics allow for modifications that can tune its properties for specific applications.
  • Research Potential: Ongoing research continues to explore the full scope of activities associated with this compound, highlighting its *importance in the development of new pharmaceuticals*. Scientists are particularly interested in its role in *targeting specific biochemical pathways*.
  • Structural Features: The benzimidazole scaffold is a unique structural feature that contributes to the compound's stability and reactivity. This fused-ring structure is not only common in many biologically active natural products but is also pivotal in enhancing *interaction dynamics* with biological receptors.

In summary, 3H-benzimidazole-5-carboxamidine stands out for its diverse *biological activities*, synthetic versatility, and potential applications in medicinal chemistry. As research continues, this compound may unveil even more exciting possibilities in the realm of drug discovery and development.

Synonyms
71892-45-0
1H-BENZIMIDAZOLE-5-CARBOXIMIDAMIDE
DTXSID30274333
3H-benzimidazole-5-carboximidamide
5-amidino benzimidazole
SCHEMBL563497
DTXCID60225813
1H-benzoimidazole-5-carboxamidine
UHGFPMUGEQINGV-UHFFFAOYSA-N
1H-1,3-benzodiazole-5-carboximidamide
1H-Benzo[d]imidazole-6-carboximidamide
PD042897
NS00069475
EN300-861937