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4,4'-Dichlorothiobenzophenone O-(4-chlorophenyl) oxime

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Identification
Molecular formula
C13H9Cl3NOS
CAS number
137-26-8
IUPAC name
1-(4-chlorophenoxy)-N-(4-chlorophenyl)methanimidothioic acid
State
State

At room temperature, 4,4'-Dichlorothiobenzophenone O-(4-chlorophenyl) oxime exists in a solid state.

Melting point (Celsius)
287.00
Melting point (Kelvin)
560.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
315.69g/mol
Molar mass
315.6880g/mol
Density
1.4255g/cm3
Appearence

4,4'-Dichlorothiobenzophenone O-(4-chlorophenyl) oxime typically appears as a crystalline solid. It is off-white to yellowish in color and may darken upon prolonged exposure to light or air.

Comment on solubility

Solubility of 1-(4-chlorophenoxy)-N-(4-chlorophenyl)methanimidothioic acid

The solubility of 1-(4-chlorophenoxy)-N-(4-chlorophenyl)methanimidothioic acid can be influenced by various factors, including its molecular structure and the presence of functional groups. As a thiol derivative, this compound generally displays specific solubility characteristics:

  • Water Solubility: This compound is likely to exhibit low to moderate solubility in water due to the hydrophobic nature of the aromatic rings, which can hinder its interaction with polar solvents.
  • Solvent Interaction: It may be more soluble in organic solvents such as dichloromethane or ethanol, where its non-polar components can interact favorably.
  • Temperature Influence: As with many chemical compounds, solubility can be temperature dependent—higher temperatures may increase solubility in certain solvents.
  • pH Sensitivity: The solubility can also change with pH, especially if there are acid-base interactions that might enhance its solubility in aqueous solutions.

In the realm of chemical compounds, it's essential to conduct empirical solubility tests to obtain precise values, since theoretical predictions may not always align with experimental data. As stated, "The structure of a molecule ultimately dictates its solubility." Understanding these properties is crucial for applications in fields such as pharmaceuticals, where solubility can significantly affect bioavailability and efficacy.


Interesting facts

Interesting Facts about 1-(4-chlorophenoxy)-N-(4-chlorophenyl)methanimidothioic acid

This compound, known as 1-(4-chlorophenoxy)-N-(4-chlorophenyl)methanimidothioic acid, is a fascinating member of the thioamide class of compounds. Here are some notable points that illustrate its significance in chemistry and potential applications:

  • Thioamide Properties: This compound features a thioamide functional group, which can make it a valuable building block in the development of pharmaceuticals and agrochemicals. Thioamides often exhibit unique biological activities.
  • Chlorophenyl Groups: The presence of chlorophenyl rings in the structure enhances its lipophilicity, which can improve the compound's ability to penetrate biological membranes. Such traits are incredibly useful in drug design.
  • Potential Uses: Compounds with similar structures have been researched for their herbicidal and antibacterial properties. As a result, studying this particular compound could unveil new applications in agriculture or medicine.
  • Analytical Chemistry: The unique structure of this compound makes it an interesting subject for analysis using spectroscopy techniques, such as NMR and IR, offering insight into its chemical behavior.
  • Research Implications: Researchers are often interested in compounds like this one for their potential to create derivatives with improved efficacy and selectivity in therapeutic applications.

In conclusion, 1-(4-chlorophenoxy)-N-(4-chlorophenyl)methanimidothioic acid is not just another compound; it represents a potential frontier in both synthetic and applied chemistry. Its structural peculiarities could pave the way for important discoveries in various scientific fields. As always, further research will be essential to uncover the full range of properties and uses of this intriguing chemical.