N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

Identification

Molecular formula

C₁₀H₁₀ClNOS₂

CAS number

.000

IUPAC name

N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

State

At room temperature, N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid is found in a solid-state, specifically a powdery or crystalline form.

Melting point (Celsius)

160.00

Melting point (Kelvin)

433.15

Boiling point (Celsius)

350.00

Boiling point (Kelvin)

623.15

General information

Molecular weight

229.78g/mol

Molar mass

229.7790g/mol

Density

1.3720g/cm³

Appearence

N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid typically appears as a crystalline solid that can vary in color. The specific color and appearance can depend on the synthesis process and purity level.

Comment on solubility

Solubility of N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

The solubility of N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid (C₁₀H₁₀ClNOS₂), like many organic compounds, can be influenced by various factors. Understanding its solubility behavior is crucial for its application in various fields such as pharmacology and agrochemicals.

Factors Affecting Solubility

Polarity: The compound possesses polar functional groups, which may enhance solubility in polar solvents such as water.
Hydrogen bonding: Potential hydrogen bonding interactions can increase solubility in protic solvents.
Temperature: Generally, an increase in temperature can improve the solubility of organic compounds.

Though specific solubility data for this compound may be limited, it is significant to note that substances containing chlorine and sulfur typically exhibit varying solubility characteristics. In practice, it is often observed that:

Solubility in water: May be moderate due to the presence of polar functional groups.
Solubility in organic solvents: Likely soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO).

In summary, while definitive solubility measurements for N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid need to be determined experimentally, one can anticipate that the combination of its structural features will allow for significant solubility in a range of solvents.

Interesting facts

Interesting Facts about N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid

N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid is a compound that exemplifies the interplay of various functional groups in organic chemistry. Here are some intriguing aspects that make this compound noteworthy:

Unique Structure: This compound features a combination of a chlorophenyl group and a thioacetamide moiety, providing a fascinating opportunity for synthetic and medicinal chemistry exploration.
Biological Relevance: Compounds with thiol and thioamide functionalities often exhibit biological activity, making them potential candidates in pharmaceuticals. Research has indicated that many thioacetamides possess antimicrobial and antifungal properties.
Environmental Impact: Chloro-substituted phenyl compounds can be relevant in assessing environmental pollutants, as their persistence and bioaccumulation tend to affect both ecosystems and human health.
Potential Applications: The dual presence of the imidothioic acid part hints at applicability in agrochemicals, particularly as herbicides or fungicides due to the reactivity of the thiol group.
Synthetic Pathways: The synthesis of such compounds often involves multi-step reactions, illustrating the complexity and creativity inherent in organic synthesis.

In summary, N-(2-chlorophenyl)-1-ethylsulfanyl-methanimidothioic acid is not just an intriguing molecular structure, but it also carries potential implications in various fields such as medicinal chemistry, environmental science, and agricultural applications. Continued research is necessary to fully understand and harness its capabilities!