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Pyridine-4-carboximidothioic acid

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Identification
Molecular formula
C6H7N2OS
CAS number
345484-84-4
IUPAC name
pyridine-4-carboximidothioic acid
State
State
At room temperature, pyridine-4-carboximidothioic acid is generally found in its solid state. It is stable under standard conditions, but care should be taken to store it in a cool, dry place to prevent any potential degradation.
Melting point (Celsius)
91.00
Melting point (Kelvin)
364.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
138.19g/mol
Molar mass
138.1890g/mol
Density
1.1900g/cm3
Appearence

Pyridine-4-carboximidothioic acid typically appears as a crystalline solid that may vary in color from white to a pale yellow, depending on the level of purity and the presence of any impurities. The solid has a characteristic odor, often associated with pyridine derivatives.

Comment on solubility

Solubility of Pyridine-4-carboximidothioic Acid

Pyridine-4-carboximidothioic acid exhibits intriguing solubility characteristics, typical of many pyridine-based compounds. Its solubility can be influenced by various factors:

  • Polarity: As a polar compound, it is expected to show good solubility in polar solvents like water and alcohols.
  • Hydrogen Bonding: The presence of the carboximidothioic group allows for potential hydrogen bonding, enhancing its solubility in polar media.
  • Temperature: Solubility often increases with temperature, so higher temperatures may promote greater dissolution in various solvents.
  • pH Levels: Modifications in pH can significantly impact the ionization of the compound, thus affecting its solubility profile.

Overall, pyridine-4-carboximidothioic acid is expected to be moderately soluble in water and various polar solvents, making it versatile for different chemical reactions and applications. As with many chemical compounds, empirical testing in specific solvents is recommended for precise solubility assessments.

Interesting facts

Interesting Facts about Pyridine-4-Carboximidothioic Acid

Pyridine-4-carboximidothioic acid is a fascinating compound that belongs to the family of carboximidothioic acids. Let’s explore some intriguing aspects of this compound:

  • Structural Uniqueness: This compound features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. The presence of this nitrogen contributes significantly to its reactivity and properties.
  • Biological Relevance: Pyridine derivatives are known to exhibit various biological activities. They can often act as intermediates in the synthesis of pharmaceuticals and agrochemicals, showcasing the diverse applications of compounds containing a pyridine structure.
  • Functional Group Influence: The carboximidothioic acid functional group in this compound can influence its acidity and reactivity, making it an intriguing subject for further study in organic synthesis.
  • Ligand Potential: The ability of the sulfur atom to coordinate with metals allows pyridine-4-carboximidothioic acid to serve as a potential ligand in coordination chemistry, facilitating the study of metal complexes.
  • Research Applications: Due to its unique structure and properties, researchers are exploring its potential applications in materials science and catalysis, further extending its significance in modern chemistry.

In summary, pyridine-4-carboximidothioic acid is more than just a chemical entity; it represents a blend of aromatic chemistry, biological potential, and the promise of new applications in various scientific fields. As we continue to investigate its properties and characteristics, who knows what exciting discoveries await in the realm of pyridine chemistry!