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Thiosemicarbazone

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Identification
Molecular formula
C10H10N4OS
CAS number
17565-81-0
IUPAC name
N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide
State
State

At room temperature, the compound typically exists as a solid.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.00
Boiling point (Celsius)
416.00
Boiling point (Kelvin)
689.00
General information
Molecular weight
206.26g/mol
Molar mass
206.2570g/mol
Density
1.3374g/cm3
Appearence

The compound appears as a pale yellow crystalline solid.

Comment on solubility

Solubility of N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide

The solubility of the compound N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide can be influenced by various factors, including its molecular structure, polarity, and the presence of functional groups. In general, the following key points can be noted about its solubility:

  • Functional Groups: This compound features multiple amine and carbonyl groups, which typically enhance solubility in polar solvents due to their ability to form hydrogen bonds.
  • Polarity: As a result of its polar functional groups, this compound is more likely to be soluble in water or polar organic solvents compared to non-polar solvents.
  • Temperature Effects: Solubility can increase with temperature; hence, higher temperatures may further facilitate the dissolution of this compound in suitable solvents.
  • pH Dependence: The solubility may also vary with pH, particularly due to the presence of amino groups that can become protonated or deprotonated depending on the acidic or basic environment.

In summary, while it is difficult to provide specific solubility values without empirical data, one can hypothesize that the solubility of N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide will be enhanced in polar solvents, and factors like temperature and pH will play a significant role in its behavior. As always, experimental determination is recommended for precise solubility data.

Interesting facts

Exploring N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide

N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide is a fascinating compound that showcases the intricate relationships between structure and function in organic chemistry. This compound belongs to a class of compounds known as thiosemicarbazones, which are notable for their diverse biological activities and potential therapeutic applications.

Interesting Facts:

  • Biological Significance: Compounds like N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide have been studied for their potential role in anti-cancer therapies. Research indicates that they may act as agents that inhibit cell proliferation.
  • Versatile Applications: This compound is being explored for its use in the field of medicinal chemistry. Its unique chemical structure allows for modifications that could enhance efficacy in drug formulations.
  • Mechanism of Action: The presence of multiple functional groups in this compound indicates a potential for coordination chemistry with metal ions. This property can be harnessed for use in designing metal-based drugs.
  • Research Potential: Ongoing studies are focusing on understanding the molecular interactions that N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide engages in, which could unveil new pathways for synthesis or therapeutic use.

As a significant representative of thiosemicarbazones, N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide indeed opens various avenues across both organic synthesis and medicinal research. The combination of the nitrogen and sulfur atoms in its structure emphasizes the importance of heteroatoms in modulating chemical and biological properties.

In conclusion, this compound not only exemplifies the beauty and complexity of organic chemistry but also fits within a larger narrative of drug discovery that aims to combat diseases through innovative chemical solutions. Keep an eye on compounds like N-[[amino(sulfanyl)methylene]amino]-4-oxo-4-phenyl-but-2-enamide as they continue to be pivotal in advancing the field!