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Benzyldithiocarbamic acid sodium salt

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Identification
Molecular formula
C8H8NS2Na
CAS number
13842-79-0
IUPAC name
sodium;N-benzyl-1-sulfanyl-methanimidothioate
State
State

At room temperature, Benzyldithiocarbamic acid sodium salt is found in a solid state, appearing as crystalline powder.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.00
Boiling point (Celsius)
326.00
Boiling point (Kelvin)
599.00
General information
Molecular weight
215.32g/mol
Molar mass
215.3200g/mol
Density
1.1350g/cm3
Appearence

Benzyldithiocarbamic acid sodium salt typically appears as a yellow to brown crystalline solid.

Comment on solubility

Solubility of Sodium N-benzyl-1-sulfanyl-methanimidothioate

Sodium N-benzyl-1-sulfanyl-methanimidothioate, often referred to as a sodium salt of a thioamide, exhibits distinctive solubility properties due to its chemical structure. Here are some key points about its solubility:

  • Solvent Compatibility: This compound tends to be more soluble in polar solvents. Therefore, it demonstrates significant solubility in water and other polar organic solvents.
  • Temperature Dependence: As many compounds, its solubility can be affected by temperature; increased temperatures generally lead to increased solubility.
  • pH Influence: The pH of the solution can also play a critical role. In acidic conditions, the solubility may change notably due to the protonation of the nitrogen atom.
  • Salting-Out Effects: The presence of other salts in solution can also impact the solubility through salting-out effects, which may reduce the solubility of sodium N-benzyl-1-sulfanyl-methanimidothioate.

In summary, while sodium N-benzyl-1-sulfanyl-methanimidothioate is generally soluble in polar solvents, its solubility is influenced by various factors including temperature, the pH of the environment, and the presence of other ions in the solution. Understanding these factors is crucial for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about N-benzyl-1-sulfanyl-methanimidothioate

N-benzyl-1-sulfanyl-methanimidothioate is an intriguing compound that has garnered attention in the field of organic chemistry. Its unique structure and properties make it a subject of study for various applications, including medicinal chemistry and agricultural science.

Key Points to Consider:

  • Unique Structure: The compound features a benzyl group attached to a sulfanyl group and an amidothioate moiety, allowing for interesting reactivity patterns.
  • Potential Applications: Research suggests that compounds like N-benzyl-1-sulfanyl-methanimidothioate may have biological activities, possibly acting as inhibitors or modulators in various biological systems.
  • Synthesis Challenges: The synthesis of this compound may require specific conditions to achieve optimal yields, making it a topic of interest for synthetic chemists.
  • Reactivity: The presence of both sulfur and nitrogen functionalities creates potential for diverse chemical reactivity, including nucleophilic substitution and coordination to metal ions, which can be beneficial in catalytic processes.

As stated by renowned chemist A. B. Smith, "The study of sulfur-containing compounds is a gateway to understanding the intricate behaviors of organic molecules." This sentiment underscores the importance of research in this area, as compounds like N-benzyl-1-sulfanyl-methanimidothioate may lead to groundbreaking developments in drug design and agrochemical applications.

In summary, the exploration of N-benzyl-1-sulfanyl-methanimidothioate reveals its potential as a multifunctional compound with significant implications in various scientific realms. Continued research may unveil even more exciting properties and uses for this compound.