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Aminoguanidinopyridinecarboxamide

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Identification
Molecular formula
C8H11N7O
CAS number
55421-27-9
IUPAC name
N-[[amino(guanidino)methylene]amino]pyridine-4-carboxamide
State
State
The compound exists in a solid state under standard conditions. It is typically found as a crystalline powder.
Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
535.00
Boiling point (Kelvin)
808.15
General information
Molecular weight
178.19g/mol
Molar mass
178.1860g/mol
Density
1.3500g/cm3
Appearence

The compound is typically a solid at room temperature, characterized by its crystalline form. It can appear as a white to off-white powder.

Comment on solubility

Solubility Characteristics

The compound N-[[amino(guanidino)methylene]amino]pyridine-4-carboxamide exhibits interesting solubility properties that are worth highlighting.

  • Water Solubility: This compound tends to have moderate to high solubility in water due to the presence of multiple polar functional groups, notably the carboxamide and guanidino groups.
  • Organic Solvents: It may exhibit varying degrees of solubility in organic solvents, which significantly depends on the specific conditions of temperature and the nature of the solvent.
  • pH Dependence: The solubility can also be influenced by pH levels, as the ionization states of the amino groups vary in different pH conditions, potentially increasing solubility in alkaline environments.
  • Hydrophobic Interactions: Considering its structural features, it might face challenges with solubility in non-polar solvents due to potential hydrophobic interactions.

In summary, while N-[[amino(guanidino)methylene]amino]pyridine-4-carboxamide is generally soluble in polar solvents, its solubility characteristics are complex and depend heavily on environmental factors such as temperature, solvent type, and pH. This multifaceted solubility behavior makes it an intriguing subject of study for applications in pharmaceuticals and other fields.

Interesting facts

Interesting Facts about N-[[amino(guanidino)methylene]amino]pyridine-4-carboxamide

N-[[amino(guanidino)methylene]amino]pyridine-4-carboxamide, often abbreviated in various ways for convenience, is a fascinating compound with several noteworthy characteristics:

  • Structural Complexity: This compound features a unique and intricate molecular structure, which combines the functionalities of both guanidine and pyridine. This complexity provides insight into its potential reactivity and interaction with biological systems.
  • Biological Relevance: The presence of the guanidine group is significant, as guanidine derivatives are widely recognized in pharmacology and biology for their roles as intermediates in the synthesis of various therapeutic agents. They often exhibit crucial enzymatic activities.
  • Potential Applications: Given its structural makeup, researchers are exploring the use of N-[[amino(guanidino)methylene]amino]pyridine-4-carboxamide in fields like drug design and development. Its capacity to engage in hydrogen bonding and other interactions can help in targeting specific biological pathways.
  • The compound's reactivity is largely attributed to the amino and guanidino groups, making it a candidate for condensation reactions, which can lead to the formation of various novel compounds.
  • Research Interests: Scientists are particularly interested in how this compound can influence enzymatic activity, potentially serving as an inhibitor or activator in metabolic pathways, which is a rich area of study in medicinal chemistry.

In summary, N-[[amino(guanidino)methylene]amino]pyridine-4-carboxamide is more than just a chemical formula; it's a compound with potential applications in medicinal chemistry, thanks to its unique structural properties and biological significance. As research progresses, it may become a key player in the development of novel therapeutic agents.

Synonyms
SCHEMBL2998343