N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₈H₈ClNO₂S₂

CAS number

86844-29-1

IUPAC name

N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid

State

At room temperature, this compound is generally found as a solid. It is stable under dry conditions and can be stored in a cool, dry place to maintain its solid state.

Melting point (Celsius)

120.00

Melting point (Kelvin)

393.15

Boiling point (Celsius)

333.00

Boiling point (Kelvin)

606.15

General information

Molecular weight

233.74g/mol

Molar mass

233.7400g/mol

Density

1.3500g/cm³

Appearence

This compound appears as an off-white to light yellow solid. It may exist in different forms based on its purification state, but generally, it is not significantly hygroscopic and remains stable under standard laboratory conditions.

Comment on solubility

Solubility of N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid

The solubility of N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is influenced by various factors, making it a compound of interest in both research and application.

Key considerations regarding its solubility include:

Polarity: The presence of polar functional groups in the molecule contributes to its solubility in polar solvents, primarily water and alcohols.
Hydrogen Bonding: Functional groups capable of forming hydrogen bonds can enhance solubility, thus allowing it to interact favorably with solvents.
Chain Length and Branching: Longer carbon chains or branched structures may hinder solubility due to increased hydrophobic interactions.

In general, **this compound may exhibit limited solubility** in non-polar solvents due to the predominance of hydrophilic features. Specifically:

In water, solubility may be **moderate**, depending on pH and temperature.
In organic solvents, solubility could **vary widely**, often requiring solvents with specific polarity characteristics to achieve dissolving.

As we consider practical applications, the solubility profile of N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid becomes crucial, especially when predicting behavior in biological systems or chemical reactions. In summary, understanding the solubility characteristics can illuminate crucial pathways for effective utilization of this compound in various scientific fields.

Interesting facts

Interesting Facts about N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid

N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid is a fascinating compound with various intriguing aspects:

Chemical Class: This compound belongs to the class of thioamides, which are known for their ability to stabilize reactive intermediates in organic reactions.
Biological Activity: The 3-chloro substitution on the phenyl ring suggests potential biological activity, making it a candidate for pharmaceutical research.
Syntheses: As a thio compound, its synthesis may involve unique pathways that leverage the reactivity of sulfur groups, which often allows for versatile functionalization.
Importance in Agrochemicals: Due to its structural characteristics, compounds like this are often explored in the development of agrochemical agents, particularly as herbicides or fungicides.
Future Applications: Research is ongoing to investigate its applications in materials science, particularly in the synthesis of novel polymers or as a precursor to more complex molecules.

In summary, N-(3-chlorophenyl)-1-methylsulfanyl-methanimidothioic acid demonstrates significant potential due to its unique chemical structure and properties. As we explore its synthesis and biological roles, we may unveil new pathways for innovative applications in both medicinal and agricultural chemistry.