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Amidinourea, 4-benzoyl-N,N-dimethyl-

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Identification
Molecular formula
C11H15N5O
CAS number
NA
IUPAC name
4-[[amino(guanidino)methylene]amino]-N,N-dimethyl-benzamide
State
State

This compound is typically encountered as a solid at room temperature.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.00
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.00
General information
Molecular weight
234.28g/mol
Molar mass
234.2760g/mol
Density
1.2300g/cm3
Appearence

The compound appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of 4-[[amino(guanidino)methylene]amino]-N,N-dimethyl-benzamide

The solubility of the compound 4-[[amino(guanidino)methylene]amino]-N,N-dimethyl-benzamide can be a fascinating topic due to its unique chemical structure and functional groups. Various factors can influence its solubility in different solvents:

  • Polarity: The polar groups present in the compound may enhance solubility in polar solvents such as water.
  • Hydrogen bonding: The presence of amino groups suggests potential for strong hydrogen bonding, which can further affect solubility.
  • Solvent type: This compound may be more soluble in organic solvents like methanol or ethanol compared to less polar solvents.
  • Temperature influence: As with many organic compounds, solubility can increase with temperature, making higher temperatures favorable for dissolving.

As a general rule, compounds with functional groups capable of forming extensive hydrogen bonds tend to exhibit higher solubility in polar solvents. Therefore, it is likely that 4-[[amino(guanidino)methylene]amino]-N,N-dimethyl-benzamide will demonstrate increased solubility in polar environments due to its structural characteristics.

In conclusion, the solubility profile of this compound underscores the interplay of molecular interactions and solvent properties, providing an intriguing area of study for further exploration.

Interesting facts

Interesting Facts about 4-[[amino(guanidino)methylene]amino]-N,N-dimethyl-benzamide

This compound exhibits fascinating properties and applications, particularly in the field of medicinal chemistry. Here are some engaging aspects worth noting:

  • Pharmaceutical Relevance: As a derivative in the class of benzenamides, it can serve as a potential lead compound for the development of new therapeutic agents. Its structural components suggest possible effects on various biological targets.
  • Amidine Influence: The presence of the guanidino group is significant since guanidines are often involved in biological functions and can mimic the action of various biomolecules, leading to enhanced interactions with enzyme systems.
  • Research Exploration: This compound is often investigated for its properties as a potential inhibitor in biochemical pathways, particularly those related to metabolism and cellular signaling.
  • Synthesis & Methods: The synthetic routes for obtaining such compounds are varied and can include methods of condensation, which are crucial for developing complex organic molecules in a lab setting.
  • Structure-Activity Relationship (SAR): Understanding how variations in the amine or guanidino parts of the structure affect biological activity can help guide the design of more potent compounds.

In summary, 4-[[amino(guanidino)methylene]amino]-N,N-dimethyl-benzamide is a noteworthy compound within organic and medicinal chemistry due to its diverse applications and effects in biological systems. The study of such compounds contributes significantly to the advancement of pharmaceutical sciences and therapeutics.