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3-Ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide

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Identification
Molecular formula
C4H7NO2S3
CAS number
55898-21-0
IUPAC name
3-ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide
State
State

At room temperature, this compound is typically a solid.

Melting point (Celsius)
71.50
Melting point (Kelvin)
344.65
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
192.29g/mol
Molar mass
192.2930g/mol
Density
1.3836g/cm3
Appearence

3-Ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide commonly appears as a solid substance. Its detailed color and crystal form can vary and should be specified based on the source or method of synthesis utilized.

Comment on solubility

Solubility of 3-ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide

The solubility of 3-ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide is an intriguing aspect that reflects its chemical nature. This compound contains both sulfur and nitrogen in its structure, which can significantly influence its interaction with solvents. Here are some insights regarding its solubility:

  • Polar vs Non-polar Solvents: Due to the presence of the 1,1-dioxide functional group, it tends to exhibit greater solubility in polar solvents such as water or alcohols compared to non-polar solvents.
  • Influence of Substituents: The ethylsulfanyl group can create a steric hindrance that might impact its solubility. The size and polarity of the group could dictate how easily the compound dissolves in various media.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature, allowing for alterations in the compound's solubility profile under different conditions.

In summary, the solubility of 3-ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide is shaped by its unique molecular structure and how it interacts with different solvents. Understanding these solubility characteristics is crucial for its applications in chemical formulations and research.

Interesting facts

Interesting Facts about 3-Ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide

3-Ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide is a fascinating compound within the realm of organosulfur chemistry. This compound features a unique thiazole ring that incorporates sulfur atoms, which contributes to its intriguing properties and applications.

Key Highlights:

  • Structural Significance: The presence of multiple sulfur atoms in its structure adds distinct chemical properties compared to more traditional carbon-based compounds. This thiazole derivative is known for its potential to form different types of reactions, showcasing the versatility of sulfur in organic chemistry.
  • Reactivity: Compounds containing dithiazole structures often exhibit interesting reactivity patterns. They can participate in various chemical transformations that can be used to synthesize more complex molecules.
  • Biological Applications: There has been research into the biological activities of thiazole compounds, which suggests potential applications in pharmaceuticals. This compound may inspire the development of new therapeutic agents.
  • Material Science: Thiazole derivatives have been explored for their role in materials science, particularly in creating new dyes and pigments due to their unique light-absorbing properties.

As a student or scientist, it is essential to recognize the invaluable potential of compounds like 3-ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide in both academic research and practical applications. The exploration of such compounds can lead to discoveries that may alter our understanding of chemistry and its contributions to technology and medicine.

To quote a famous chemist, "The beauty of chemistry lies in its complexity and the unexpected solutions that emerge from even the simplest of compounds."
This reinforces the idea that every compound, no matter how obscure, holds the seeds of innovation waiting to be discovered.

Synonyms
18137-09-2
1,3,4-DITHIAZOLE, 5-ETHYLTHIO-, 3,3-DIOXIDE
BRN 1073385
5-Ethylmercapto-1,3,4-dithiazol-3-dioxide
DTXSID60171129
DTXCID1093620
3-ethylsulfanyl-1,4,2-dithiazole 1,1-dioxide
3-(Ethylthio)-1,4,2-dithiazole 1,1-dioxide