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N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid

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Identification
Molecular formula
C15H14N2O2S2
CAS number
13467-07-3
IUPAC name
N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid
State
State

The compound is typically found as a solid at room temperature. This state is consistent with many aromatic compounds of similar molecular weight, particularly those containing sulfur and aromatic rings.

Melting point (Celsius)
117.00
Melting point (Kelvin)
390.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
302.35g/mol
Molar mass
302.3450g/mol
Density
1.3200g/cm3
Appearence

The compound typically appears as a yellow crystalline solid. Its crystalline nature and the yellow hue are indicative of an aromatic compound with nitro functional group influences, giving it distinct coloration.

Comment on solubility

Solubility of N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid

The solubility of N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid, a complex organic compound, can present some intriguing characteristics. Understanding its solubility is essential for various applications in chemistry and pharmaceuticals. Here are some factors to consider:

  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents, while its hydrophobic benzyl and nitrophenyl moieties may hinder solubility in water.
  • Temperature: General solubility tends to increase with temperature, which can aid in dissolving compounds that are otherwise poorly soluble at lower temperatures.
  • pH Effects: Being a thio-imidothioic acid, changes in pH could significantly impact solubility due to protonation and deprotonation behaviors.
  • Solvent Choice: It is critical to choose the right solvent; for example, solvents like DMSO or DMF may dissolve this compound better than water.

In summary, solubility will greatly depend on the specific conditions and the medium utilized. As noted, “the solution of a substance is a balance of its molecular structure and the solvent properties,” highlighting how the intricate design of N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid influences its ability to dissolve in various environments.

Interesting facts

Interesting Facts about N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid

N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid is a fascinating compound that showcases the intricate interplay between organic chemistry and medicinal applications. This compound is known for several intriguing attributes:

  • Unique Structure: The combination of a benzyl group with nitrophenyl and thioic acid functionalities contributes to its distinctive chemical behavior and potential reactivity.
  • Bioactivity: Compounds like this one are often explored for their bioactive properties. The presence of the nitro group may confer specific biological activities that can be harnessed in drug development.
  • Applications in Research: Due to its versatile structure, this compound can serve as a valuable intermediate in organic synthesis and medicinal chemistry.
  • Potential for Derivatives: Researchers can modify various functional groups attached to this compound to explore new derivatives that could enhance efficacy or reduce toxicity.
  • Thioic Acid Domain: The thioic acid moiety is of particular interest, as thio compounds often exhibit unique reactivity patterns and can participate in various reactions, including nucleophilic substitutions.

As stated in the words of renowned chemist "The beauty of chemistry lies in the diversity of compounds and their potential to address real-world challenges."

Overall, N-benzyl-1-[(4-nitrophenyl)methylsulfanyl]methanimidothioic acid represents an intriguing area of study in both organic chemistry and pharmacology, highlighting the potential for discovery within complex molecular structures.