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Thiobis(acetylene)

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Identification
Molecular formula
C5H10OS2
CAS number
39195-62-7
IUPAC name
bis(ethylsulfanyl)methanone
State
State

At room temperature, bis(ethylsulfanyl)methanone is in the liquid state. It is important to handle it under controlled conditions to prevent any reaction due to its reactive potential.

Melting point (Celsius)
-44.50
Melting point (Kelvin)
228.50
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.00
General information
Molecular weight
120.18g/mol
Molar mass
120.1800g/mol
Density
1.0460g/cm3
Appearence

The compound presents as a colorless liquid. In its pure form, the liquid is clear and devoid of any significant coloration, often characterized by its strong sulfur-like smell.

Comment on solubility

Solubility of bis(ethylsulfanyl)methanone

When examining the solubility of bis(ethylsulfanyl)methanone, it is important to consider the following factors:

  • Polarity: The presence of the ethylsulfanyl groups contributes to the overall polarity of the molecule, which can influence its solubility in various solvents.
  • Solvent Compatibility: bis(ethylsulfanyl)methanone is likely to be soluble in polar organic solvents such as ethanol or acetone, but may show limited solubility in non-polar solvents because of its polar groups.
  • Temperature Effects: Solubility can vary with temperature; typically, an increase in temperature may enhance solubility for many organic compounds, including bis(ethylsulfanyl)methanone.
  • Impact of Functional Groups: The ethylsulfanyl groups can undergo interactions, such as hydrogen bonding, that may foster favorable solubility profiles in situations where such interactions enhance dissolution in specific solvents.

In conclusion, the solubility of bis(ethylsulfanyl)methanone is primarily influenced by its molecular structure, polarity, and the nature of the solvent used. Solubility tests should always be conducted under controlled conditions to understand the specific behavior of this compound in different environments.

Interesting facts

Interesting Facts about Bis(ethylsulfanyl)methanone

Bis(ethylsulfanyl)methanone, often recognized for its unique structure, is a fascinating compound in the realm of organic chemistry. Here are some key points to appreciate about this intriguing compound:

  • Functional Group Diversity: The compound contains both a ketone and thioether groups, which can influence its chemical reactivity and the types of reactions it can participate in.
  • Synthesis Routes: Due to its complex structure, bis(ethylsulfanyl)methanone can be synthesized through various methods, including the reaction of appropriate thioacetates with ketones. This showcases the creativity required in synthetic organic chemistry.
  • Applications: Compounds with similar structures often find applications in pharmaceuticals and agrochemicals, providing insight into how bis(ethylsulfanyl)methanone might serve as a starting point for further chemical development.
  • Research Potential: This compound provides a rich platform for exploring reactivity, functionalization, and potential applications in materials science, particularly in developing new methods of synthesis or catalytic processes.
  • Environmental Considerations: The study of thiol and thioether compounds is essential in understanding their environmental impact, especially since many sulfur-containing compounds can play significant roles in biochemical pathways.

As a student or scientist delving into the world of bis(ethylsulfanyl)methanone, one can appreciate the balance between synthetic challenges and the potential for innovative applications. Perhaps the most compelling aspect of this compound lies in its ability to act as both a product and a reactant within broader chemical networks.

In the words of chemists, “The beauty of chemistry lies in its complexity and interconnectedness.” Bis(ethylsulfanyl)methanone is a small yet significant example of this principle.

Synonyms
623-80-3
S,S'-Diethyl Dithiocarbonate
S,S-DIETHYL CARBAMODITHIOATE
bis(ethylsulfanyl)methanone
DITHIOCARBONIC ACID S,S-DIETHYL ESTER
Dithiocarbonic Acid S,S'-Diethyl Ester
S,S-Diethyl dithiocarbonate
S,S-DIETHYL CARBONODITHIOATE
MFCD00144162
Carbonodithioic acid, S,S-diethyl ester
Carbonic acid, dithio-, S,S-diethyl ester
SCHEMBL3065037
DTXSID50211366
AKOS006230608
FD61295
D2078
T71137