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N-ethyl-s-phenylisothiourea

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Identification
Molecular formula
C9H11ClN2S2
CAS number
5387-92-4
IUPAC name
N-(4-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid
State
State

The compound exists as a solid at room temperature. It remains stable and does not sublimate under normal atmospheric conditions. Its stability makes it easy to handle in laboratory settings.

Melting point (Celsius)
85.20
Melting point (Kelvin)
358.35
Boiling point (Celsius)
251.50
Boiling point (Kelvin)
524.65
General information
Molecular weight
282.86g/mol
Molar mass
282.8600g/mol
Density
1.3456g/cm3
Appearence

The compound appears as a beige to light brown crystalline powder. It is not hygroscopic and remains stable under normal storage conditions. The compound does not emit any significant odor.

Comment on solubility

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

N-(4-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid is a complex compound, and its solubility can greatly influence its applications in various fields. Understanding its solubility is crucial for effective usage and handling. Here are some key points regarding the solubility of this compound:

  • Solvent Compatibility: This compound is expected to have varying solubility in different solvents. Generally, organic solvents like ethanol, dimethyl sulfoxide (DMSO), and acetonitrile may show higher solubility due to their polar aprotic nature.
  • pH Sensitivity: The solubility may also be affected by the pH of the solution. In acidic or basic environments, the protonation or deprotonation of functional groups can alter solubility.
  • Temperature Influence: Like many other compounds, increasing the temperature can generally enhance solubility. This is particularly significant for many organic compounds.
  • Functional Groups Impact: The presence of the -NH and -SH groups suggests that hydrogen bonding may play a role in solubility behavior, potentially increasing solubility in polar solvents.

In summary, the solubility of N-(4-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid can be influenced by several factors such as solvent type, pH, temperature, and the compound's functional groups. Understanding these interactions is essential for optimizing its use in practical applications.

Interesting facts

Interesting Facts About N-(4-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

The compound N-(4-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid is a fascinating example of a diverse and versatile chemosynthetic compound. Here are some engaging aspects of this compound:

  • Biological Activity: This compound is particularly notable for its potential biological activities. Many derivatives in this class have been explored for their roles in pharmacology, potentially offering therapeutic effects.
  • Synthesis: The synthesis of this compound showcases the beauty of organic chemistry. The incorporation of a sulfenyl group through a series of reactions highlights the importance of functional group manipulation in creating active molecules.
  • Research Interest: The scientific community is actively researching the structure-activity relationship (SAR) of compounds like this one. Understanding how slight modifications can impact their efficacy and potency opens avenues for drug development.
  • Environmental Relevance: Compounds similar to N-(4-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid are often studied for their environmental impact, particularly in pesticide formulations, showcasing the importance of chemistry in agricultural applications.
  • Functional Versatility: The presence of both an amine and thioester functionality makes this compound a potential building block for a variety of further chemical syntheses, representing the adaptability of compounds in synthetic organic chemistry.

As a research chemist or student, one could appreciate not only the compound's structural complexity but also the implications it holds for both pharmaceuticals and agrochemicals. Its study serves as a reminder of how intricate changes at the molecular level can lead to vastly different biological and chemical properties, prompting a deeper exploration into the world of chemical compounds.