1-ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid

Identification

Molecular formula

C₁₀H₁₂N₂O₃S₂

CAS number

Not Available

IUPAC name

1-ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid

State

At room temperature, 1-ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid is a crystalline solid. Its structure is characterized by high stability in this solid state.

Melting point (Celsius)

176.00

Melting point (Kelvin)

449.00

Boiling point (Celsius)

336.00

Boiling point (Kelvin)

609.00

General information

Molecular weight

272.36g/mol

Molar mass

272.3570g/mol

Density

1.3200g/cm³

Appearence

1-Ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid appears as a yellow crystalline solid. Its vibrant color and crystal structure make it distinctive among similar organosulfur compounds. It is often utilized in research settings where detailed observation of its crystalline nature is necessary.

Comment on solubility

Solubility of 1-Ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic Acid

The solubility of 1-ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid (C₁₀H₁₂N₂O₃S₂) can be complex and is influenced by various factors. Here are some important points to consider:

Polarity: The presence of polar functional groups such as the nitrophenyl and amidothioic components suggests that the compound may possess some degree of polarity, which can enhance solubility in polar solvents like water.
Hydrogen Bonding: The functional groups may also engage in hydrogen bonding, further affecting solubility. This characteristic can lead to increased solubility in aqueous environments.
Solvent Interaction: As with many organic compounds, solubility will be influenced by the choice of solvent. For example:

In polar solvents such as water, the compound may exhibit moderate to high solubility.
In organic solvents like chloroform or hexane, solubility may be lower due to the increased hydrophobic character.

While experimental data would provide the most accurate insight into the actual solubility values, predicting solubility often involves a combination of theoretical understanding and empirical results. Ultimately, the solubility of 1-ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid may vary based on environmental conditions and solvent choices.

Interesting facts

Interesting Facts about 1-Ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic Acid

This fascinating compound, 1-ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid, showcases a unique structural combination that opens doors to diverse applications in the field of chemistry. Here are some intriguing aspects worth exploring:

Structural Diversity: The presence of both a nitrophenyl group and a thioic acid function gives this compound a distinct reactivity profile, making it an excellent candidate for further chemical synthesis.
Biological Implications: Compounds with a nitrophenyl moiety often demonstrate interesting biological activities, such as potential antibacterial or antitumor properties, making them relevant in pharmaceutical research.
Environmental Significance: The study of thiol compounds has garnered attention due to their roles in environmental chemistry, particularly in relation to their ability to form complexes with heavy metals.
Versatile Applications: Given its structural characteristics, this compound could be used in various fields including agrochemicals, where it may serve as a precursor or an intermediate for pesticide synthesis.
Research Potential: The novel structure of this compound invites further exploration, potentially leading to the discovery of new reactions or applications in organic synthesis.

In the words of chemist Gilbert N. Lewis, "The greatest discoveries are those that help the world." Engaging with compounds like 1-ethylsulfanyl-N-(4-nitrophenyl)methanimidothioic acid brings us one step closer to unlocking new scientific innovations.