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1-Ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid

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Identification
Molecular formula
C15H15NO2S2
IUPAC name
1-ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid
State
State

This compound is a solid at room temperature. It is typically handled as a powder.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.00
Boiling point (Celsius)
278.00
Boiling point (Kelvin)
551.00
General information
Molecular weight
339.45g/mol
Molar mass
339.4480g/mol
Density
1.2860g/cm3
Appearence

The compound appears as a pale yellow powder. It may also have a slight odor characteristic of thioesters or related sulfur compounds.

Comment on solubility

Solubility of 1-ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid

The solubility of 1-ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid can be intriguing given its complex structure. Understanding its solubility characteristics is essential, especially in the context of chemical applications. Here are some key points to consider:

  • Polarity: The presence of both a sulfur atom and an ethoxycarbonyl group contributes to a mixed polarity, affecting its interaction with solvents. Generally, polar compounds tend to be more soluble in polar solvents.
  • pH Dependence: The solubility may be influenced by pH levels, particularly due to the acidic nature of the compound. Changes in pH can lead to protonation or deprotonation, altering solubility.
  • Solvent Preferences: While exact solubility data may be limited, compounds with similar functional groups often exhibit higher solubility in organic solvents like ethanol or dimethyl sulfoxide (DMSO). Therefore, it could be expected that 1-ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid demonstrates solubility in such solvents.
  • Temperature Influence: Solubility often increases with temperature, a factor that could be significant for this compound, particularly during experimental procedures.

In conclusion, while the precise solubility of 1-ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid may require empirical determination, considerations of its polarity, pH sensitivity, solvent compatibility, and temperature effects provide valuable guidelines for predicting its behavior in various environments.

Interesting facts

Interesting Facts about 1-ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid

This intriguing compound belongs to the class of thioic acids, where sulfur plays a pivotal role in the chemical structure, imparting unique properties and behaviors. The compound combines several functional groups, which makes it a subject of interest in various fields of chemistry, including organic synthesis and medicinal chemistry.

Chemical Features and Structure

  • Thioic Acid Focus: As a thioic acid derivative, it showcases the versatility of sulfur in organic compounds, introducing functionalities that carbon alone cannot provide.
  • Functional Diversity: This compound features an ethoxycarbonyl group and a naphthyl moiety, which can enhance reactivity and influence the compound's physical properties.
  • Sulfur's Role: Sulfur atoms often contribute to the biological activity of compounds, making this thioic acid derivative worthy of examination for potential pharmacological effects.

Applications and Research Potential

The exploration of this compound opens avenues for further scientific study:

  • Medicinal Chemistry: With its unique structural components, it may serve as a precursor for developing new drugs, particularly in the realm of anticancer or antimicrobial agents.
  • Organic Synthesis: The structural motifs present may facilitate reactions that introduce further complexity into organic frameworks, valuable for chemical synthesis.

In essence, 1-ethoxycarbonylsulfanyl-N-(1-naphthyl)methanimidothioic acid is more than just a molecular assembly; it represents a treasure trove of opportunity for scientists to uncover new properties, reactions, and potential applications. As researchers delve deeper into its synthesis and reactivity, the implications of this compound could resonate across various disciplines in chemistry.