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Methidathion

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Identification
Molecular formula
C6H11NO4PS3
CAS number
950-37-8
IUPAC name
sodium;N-(1-phenylethyl)-1-sulfanyl-methanimidothioate
State
State

At room temperature, Methidathion is a solid.

Melting point (Celsius)
38.00
Melting point (Kelvin)
311.15
Boiling point (Celsius)
227.00
Boiling point (Kelvin)
500.15
General information
Molecular weight
302.39g/mol
Molar mass
302.3910g/mol
Density
1.2800g/cm3
Appearence
Methidathion typically appears as a white crystalline solid.
Comment on solubility

Solubility of Sodium N-(1-phenylethyl)-1-sulfanyl-methanimidothioate

The solubility of sodium N-(1-phenylethyl)-1-sulfanyl-methanimidothioate is an important factor to consider in both research and practical applications. This compound, featuring a thiol and an amidine functional group, may exhibit a range of solubility characteristics depending on the medium it is placed in. Here are some key points to understand about its solubility:

  • Polarity: The presence of the polar sulfanyl (-SH) and amidine (-C(NH)NH2) groups suggests that sodium N-(1-phenylethyl)-1-sulfanyl-methanimidothioate has the potential to be soluble in polar solvents like water.
  • Interaction with Water: The ionic nature due to the sodium (Na+) cation promotes interaction with water molecules, further enhancing its solubility.
  • Influence of Temperature: As with many compounds, solubility may increase with temperature, which is critical for applications requiring higher concentrations or specific solubility behaviors.
  • pH Sensitivity: The solubility might also be affected by pH levels; the amidine functionality could lead to changes in ionization states that impact solubility.

In general, one might expect sodium N-(1-phenylethyl)-1-sulfanyl-methanimidothioate to be moderately soluble in water, but it's always advisable to conduct empirical tests in various solvents to ascertain precise solubility values. Understanding the solubility profile of such a compound is crucial for optimizing its use in various chemical and biological applications.

Interesting facts

Interesting Facts about N-(1-phenylethyl)-1-sulfanyl-methanimidothioate

N-(1-phenylethyl)-1-sulfanyl-methanimidothioate is a unique chemical compound with a variety of intriguing properties and applications. Here are some interesting aspects that make this compound worth studying:

  • Thioester Backbone: The presence of a thioester functional group in its structure provides this compound with remarkable reactivity, allowing it to participate in various organic synthesis reactions.
  • Aromatic Influence: The phenyl group contributes to the compound's stability and potential biological activity, making it a subject of interest in medicinal chemistry.
  • Versatile Synthetic Utility: It can be utilized in synthesis pathways to create derivatives with different biological or chemical properties, adapting its functionality for different applications.
  • Biological Relevance: Compounds similar to this structure have been noted in research for their potential antitumor, antimicrobial, and anti-inflammatory activity, suggesting valuable applicability in pharmaceuticals.
  • Soft Lewis Acid: The sulfur atom in the thiol group acts as a soft Lewis acid, which can aid in catalysis through coordination with other electron-rich centers.

As a scientist or student exploring this compound, one might consider how the **interaction of functional groups** affects its reactivity and biological properties.

In summary, N-(1-phenylethyl)-1-sulfanyl-methanimidothioate exemplifies the complex interplay between structure and function. It serves as an excellent study reference for aspiring chemists interested in organic synthesis, medicinal applications, and the diverse chemistry of sulfur-containing compounds.