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Fenothiocarb

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Identification
Molecular formula
C9H10NS2
CAS number
124754-01-8
IUPAC name
1-methylsulfanyl-N-phenyl-methanimidothioic acid
State
State

At room temperature, Fenothiocarb exists as a solid. Due to its stable crystalline structure, it remains solid under typical environmental conditions until it reaches its melting point.

Melting point (Celsius)
87.00
Melting point (Kelvin)
360.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
215.34g/mol
Molar mass
215.3360g/mol
Density
1.2100g/cm3
Appearence

Fenothiocarb appears as a solid in its pure form. It typically presents itself in a crystalline state and may range from a yellow to a pale brown color. Its appearance can vary slightly based on purity and environmental conditions.

Comment on solubility

Solubility of 1-methylsulfanyl-N-phenyl-methanimidothioic acid

1-methylsulfanyl-N-phenyl-methanimidothioic acid, with its complex structure, exhibits intriguing solubility characteristics. Its solubility can be influenced by several factors:

  • Polarity: The presence of sulfonyl and phenyl groups introduces polarity, which generally enhances solubility in polar solvents.
  • Hydrogen Bonding: The carboxylic acid functional group may allow for intramolecular and intermolecular hydrogen bonding, affecting its dissolution in different solvents.
  • Solvent Interactions: This compound is likely to be more soluble in polar protic solvents, such as water or methanol, due to the ability of the solvent to solvate the ionic and polar moieties.
  • Temperature Effect: As with many chemical compounds, solubility may increase with higher temperatures, allowing for better dissolution.

In summary, while specific solubility data may not be readily available, the unique structural features of 1-methylsulfanyl-N-phenyl-methanimidothioic acid suggest that it will have limited solubility in nonpolar solvents and relatively better solubility in polar solvents. This variance in solubility is an essential consideration when determining its suitability for various chemical applications.

Interesting facts

Interesting Facts about 1-methylsulfanyl-N-phenyl-methanimidothioic acid

1-methylsulfanyl-N-phenyl-methanimidothioic acid, also known by its various systematic names, is a fascinating compound that falls within the category of thioacids and thioamides. Here are some intriguing aspects to consider:

  • Structural Diversity: This compound features a structure that integrates both sulfur and nitrogen functionalities, contributing to its unique chemical properties. The presence of the methylsulfanyl group adds to its potential reactivity.
  • Potential Applications: Compounds of this type may have relevance in medicinal chemistry and agricultural chemistry, particularly as potential agents for pest control or as intermediates in the synthesis of more complex molecules.
  • Synthesis Challenges: The synthesis of 1-methylsulfanyl-N-phenyl-methanimidothioic acid presents challenges due to its complex structure, which often requires specialized reagents and conditions in the laboratory.
  • Reactivity: As a thioacid, it may demonstrate unique reactivity patterns compared to conventional carboxylic acids, potentially allowing it to form thiol esters or react in nucleophilic substitution reactions.
  • Research Potential: The study of compounds like this one can lead to a greater understanding of sulfur-containing organic compounds, which are critical in various biochemical processes and industrial applications.

In the words of a prominent chemist, "The nature of a compound lies not just in its composition, but in the stories it tells through its reactions and properties." For students and researchers alike, exploring 1-methylsulfanyl-N-phenyl-methanimidothioic acid can be an exciting endeavor that bridges theoretical knowledge and practical application.