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Dazomet

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Identification
Molecular formula
C5H10N2OS2
CAS number
533-74-4
IUPAC name
3-(dimethoxyphosphinothioylsulfanylmethyl)-5-methylsulfanyl-1,3,4-thiadiazol-2-one
State
State

At room temperature, Dazomet is in a solid state.

Melting point (Celsius)
104.00
Melting point (Kelvin)
377.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
162.23g/mol
Molar mass
162.2290g/mol
Density
1.5200g/cm3
Appearence

Dazomet appears as a colorless crystalline solid.

Comment on solubility

Solubility of 3-(dimethoxyphosphinothioylsulfanylmethyl)-5-methylsulfanyl-1,3,4-thiadiazol-2-one

The solubility of 3-(dimethoxyphosphinothioylsulfanylmethyl)-5-methylsulfanyl-1,3,4-thiadiazol-2-one in various solvents can significantly impact its practical applications and effectiveness. Notably, here are some considerations regarding its solubility:

  • Polarity and Structure: The presence of dimethoxy groups and sulfur atoms may enhance its solubility in polar solvents, whereas the thiadiazole framework might limit solubility in non-polar solvents.
  • Solvent Dependency: The solubility can vary widely depending on the solvent used:
    • Water: Limited solubility might be expected due to its complex structure.
    • Organic Solvents: Compounds such as ethanol or acetone could potentially dissolve it better.
  • Temperature Influence: As with many compounds, increasing temperature might improve solubility, making it more feasible for use in various reactions.
  • pH Considerations: The solubility could also be affected by the pH of the solution, particularly if the compound has ionizable groups.

Understanding the solubility of this compound is crucial for developing effective formulations and ensuring its optimal performance in various chemical applications. Always consult specific studies or solubility charts for precise data.

Interesting facts

Interesting Facts about 3-(dimethoxyphosphinothioylsulfanylmethyl)-5-methylsulfanyl-1,3,4-thiadiazol-2-one

This fascinating compound belongs to the family of thiadiazoles, which are known for their diverse biological activities and applications in various fields. Here are some captivating facts about this complex structure:

  • Versatile Building Block: Thiadiazoles are often used as a key structural unit in the synthesis of pharmaceuticals, agrochemicals, and materials science, showcasing their versatility in different chemical environments.
  • Biological Activity: Compounds containing thiadiazole rings have been documented for their antimicrobial, antifungal, and anti-inflammatory properties, making them significant in medicinal chemistry.
  • Pivotal Role of Phosphorus: The presence of the dimethoxyphosphinothioyl group points to potential applications in developing pesticides and herbicides, demonstrating the role of phosphorus in enhancing pesticide efficacy.
  • Sulfanylmethyl Group: This specific substitution may contribute to improving the structure-activity relationship of the compound, which is critical in optimizing performance in biological assays.
  • Research Potential: As a relatively novel compound, it opens up avenues for research into new chemical reactions and interactions, especially in the context of organic synthesis methodologies.

In summary, the multifaceted nature of 3-(dimethoxyphosphinothioylsulfanylmethyl)-5-methylsulfanyl-1,3,4-thiadiazol-2-one not only highlights its importance in the chemical landscape but also marks its potential as a precursor for valuable derivatives. The blend of sulfur and phosphorus chemistry encapsulated in this compound drives ongoing exploration and innovation in pharmaceuticals and agrochemicals.

Synonyms
13432-51-4
GS 13002
O,O-Dimethyl S-((5-(methylthio)-2-oxo-1,3,4-thiadiazol-3(2H)-yl)methyl) phosphorodithioate
DTXSID70158643