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
Molecular Weight
278.40g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2000g/cm3
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.

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