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N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid

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Identification
Molecular formula
C13H17N5S
CAS number
Not available
IUPAC name
N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid
State
State

The compound is typically a solid at room temperature, characterized by its firm crystalline structure.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.00
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.00
General information
Molecular weight
278.40g/mol
Molar mass
278.4010g/mol
Density
1.2000g/cm3
Appearence

N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid typically appears as a crystalline solid. The color of these crystals can vary but it is generally observed to have a light coloration.

Comment on solubility

Solubility of N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid

N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid is a complex organic compound characterized by its unique structure, which influences its solubility in various solvents. The solubility of this compound can be affected by several factors:

  • Polarity: The presence of polar groups in its structure can lead to solubility in polar solvents, such as water or alcohols.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvent molecules often enhances solubility. This compound, due to its functional groups, has the potential to engage in such interactions.
  • Temperature: Solubility can significantly increase with temperature for many compounds. Thus, heating a solution may promote greater solubility.
  • pH of the Solution: Variations in pH can alter the ionization of acidic or basic functional groups, affecting solubility in aqueous solutions.

It is important to note that while theoretical considerations point to potential solubility traits, empirical study is necessary to ascertain exact solubility limits and behavior in different environments. As a general rule, "like dissolves like," meaning that compounds with similar polarities and functional groups will dissolve more readily in each other.

In summary: Solubility details for N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid warrant further investigation to determine its practical applications and behavior in various chemical contexts.

Interesting facts

N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid

N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid is an intriguing compound that presents a range of fascinating properties and potential applications. Known primarily for its role in organic synthesis, this compound features several key characteristics that make it noteworthy:

  • Versatile Intermediates: Due to its unique structure, this compound acts as a significant intermediate in various chemical reactions, including the formation of more complex organic molecules.
  • Biological Activity: Compounds bearing the azepane ring are often researched for their biological activities, making them of interest in medicinal chemistry.
  • Research Applications: Its distinctive thioic acid functional group could be leveraged in the development of new pharmaceuticals or agrochemicals, showcasing its potential in applied chemistry.
  • Metal Coordination: The nitrogen groups in the pyridyl and carbohydrazone structures may facilitate coordination with metal ions, opening pathways for the creation of metal-organic frameworks or catalysts.

Furthermore, the study of compounds like N-(2-pyridylmethylene)azepane-1-carbohydrazonothioic acid enhances our understanding of structural diversity in organic compounds. The hydrazone linkage within its framework often exhibits *E/Z isomerism*, adding another layer of complexity to its chemical behavior and reactivity.

As researchers delve deeper into its properties, we may uncover novel methodologies for utilizing this compound in various industrial applications or therapeutic contexts, thus continuing the legacy of innovation within the field of organic chemistry.