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3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide

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Identification
Molecular formula
C6H8ClN7O
CAS number
82625-39-0
IUPAC name
3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide
State
State

At room temperature, 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide is a solid substance.

Melting point (Celsius)
228.50
Melting point (Kelvin)
501.65
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
231.59g/mol
Molar mass
231.5870g/mol
Density
2.1000g/cm3
Appearence

The compound typically appears as a crystalline solid. It is generally white to off-white in color and may exhibit some crystalline luster due to its crystalline structure.

Comment on solubility

Solubility of 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide

The solubility of 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide is influenced by several factors, mainly its chemical structure and interactions with solvents.

Factors Affecting Solubility

  • Polarity: The presence of amino and guanidino functional groups suggests a higher likelihood of solubility in polar solvents.
  • Hydrogen Bonding: This compound can form hydrogen bonds, enhancing its affinity for water and similar solvents.
  • Temperature: As with many compounds, solubility may increase with temperature, enabling greater interaction with the solvent molecules.

In summary, while the specific solubility data may vary, one could expect 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide to be relatively soluble in polar solvents due to its functional groups that promote solvation. As the saying goes, "Like dissolves like," indicating that compounds with similar polarities tend to be more soluble together.

Interesting facts

Interesting Facts about 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide

3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide is a fascinating compound that attracts attention due to its unique structural features and potential applications. Here are some intriguing aspects:

  • Bioactivity: This compound belongs to a class of molecules that exhibit significant biological activity, making them of interest in medicinal chemistry. Its structure suggests potential use as a pharmacological agent in various therapeutic areas.
  • Structural Insights: The presence of both amino and guanidino functional groups gives this compound unique reactivity and interaction capabilities that can be crucial in designing new drugs or agrochemicals.
  • Research Potential: The compound serves as a lead structure for synthesis and modification, opening the door for researchers to explore derivatives that may enhance efficacy or reduce toxicity.
  • Chlorine Atom: The incorporation of a chlorine atom can alter the lipophilicity and metabolic stability of the molecule, factors that are critical in the optimization process of drug development.

As scientists, the exploration of compounds like 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide not only broadens our understanding of chemical interactions but also contributes to advancements in therapeutic methodologies. Exploring its interplay within various biological systems continues to inspire ongoing research in the field.


Overall, the journey into the world of this compound exemplifies the intersection of chemistry, biology, and pharmacology, showcasing how fundamental research can lead to groundbreaking discoveries.

Synonyms
3-Amino-6-chloropyrazinamidoguanidine
PK8445UJX4
UNII-PK8445UJX4
1458-04-4
Pyrazinecarboxylic acid, 3-amino-6-chloro-, 2-amidinohydrazide
2-Pyrazinecarboxylic acid, 3-amino-6-chloro-, 2-(aminoiminomethyl)hydrazide
DTXSID201149203
3-Amino-6-chloro-2-pyrazinecarboxylic acid 2-(aminoiminomethyl)hydrazide