Skip to main content

S-(thiiran-2-ylmethyl) ethanethioate

ADVERTISEMENT
Identification
Molecular formula
C6H10OS2
CAS number
13137-77-4
IUPAC name
S-(thiiran-2-ylmethyl) ethanethioate
State
State

At room temperature, S-(thiiran-2-ylmethyl) ethanethioate is typically a liquid. Its state is due to its relatively low melting point, keeping it in a liquid state under standard conditions.

Melting point (Celsius)
-51.00
Melting point (Kelvin)
222.15
Boiling point (Celsius)
236.00
Boiling point (Kelvin)
509.15
General information
Molecular weight
148.24g/mol
Molar mass
148.2400g/mol
Density
1.0700g/cm3
Appearence

S-(thiiran-2-ylmethyl) ethanethioate appears as a transparent or light yellow liquid. It might present a viscous texture, often associated with its thiirane (epoxy-thio) functionality. The thiirane ring can give it a characteristic odor, especially common in sulfur-containing organic compounds.

Comment on solubility

Solubility of S-(thiiran-2-ylmethyl) ethanethioate

S-(thiiran-2-ylmethyl) ethanethioate exhibits a unique profile when it comes to solubility, particularly in polar and non-polar solvents. Understanding its solubility can reveal much about its potential applications and interactions in various environments.

Key Points on Solubility:

  • Polar Solvents: S-(thiiran-2-ylmethyl) ethanethioate tends to have decent solubility in polar solvents such as water and alcohols. This is primarily due to the presence of the thiol (–SH) group, which can form hydrogen bonds with water molecules.
  • Non-Polar Solvents: Conversely, it may show lower solubility in non-polar solvents due to its polar functional groups, which are less compatible with the hydrophobic nature of non-polar solvents.
  • Temperature Sensitivity: The solubility can also change with temperature; increasing temperature usually enhances solubility for most compounds, and this may apply to S-(thiiran-2-ylmethyl) ethanethioate.
  • pH Dependency: Variations in the pH of the solvent can significantly impact solubility, as changes in protonation states of the functional groups may occur.
  • Application Considerations: The solubility characteristics of this compound make it particularly useful in formulations and chemical reactions where the interaction with other polar entities is crucial.

In summary, the solubility of S-(thiiran-2-ylmethyl) ethanethioate reflects its chemical structure and functional groups, making it an interesting compound for various applications. Understanding these solubility properties can aid in predicting its behavior in practical scenarios.

Interesting facts

Interesting Facts About S-(thiiran-2-ylmethyl) ethanethioate

S-(thiiran-2-ylmethyl) ethanethioate is a fascinating compound with a unique structure that warrants further exploration. Here are some intriguing aspects of this compound:

  • Structural Features: The presence of the thiirane ring in its structure plays a significant role in its chemical reactivity and properties. Thiiranes are known for their ability to undergo ring-opening reactions, making them valuable in synthetic organic chemistry.
  • Biological Relevance: Compounds containing thiirane groups have been observed to exhibit interesting biological properties, some of which may lead to potential pharmaceutical applications. This highlights the significance of studying such structures.
  • Thiolester Linkage: The ethanethioate portion indicates that this compound may behave similarly to other thioesters, which are often involved in biochemical pathways, including those relevant to metabolism and esterification reactions.
  • Synthetic Utility: Due to its unique structure, S-(thiiran-2-ylmethyl) ethanethioate may serve as a versatile intermediate in organic synthesis, providing pathways to more complex molecules.
  • Potential Applications: Its reactivity opens up possibilities for various applications, ranging from materials science to medicinal chemistry, which can make it a compound of interest for ongoing research.

Exploring the properties and reactions of S-(thiiran-2-ylmethyl) ethanethioate could uncover new dimensions in the realm of organic chemistry. Scientists and students alike can appreciate how such compounds enhance our understanding of molecular behavior and contribute to the advancement of chemical sciences.

Synonyms
Thioacetic acid S-2,3-epithiopropyl ester
25435-29-4
BRL 459
BRN 0107721
Ethanethioic acid, S-(thiiranylmethyl) ester
ACETIC ACID, THIO-, S-2,3-EPITHIOPROPYL ESTER
5-17-03-00054 (Beilstein Handbook Reference)
RefChem:316698
S-(thiiran-2-ylmethyl) ethanethioate
SCHEMBL11573449
DTXSID30948300
1-(Thiiran-2-ylmethylthio)ethan-1-one
S-[(Thiiran-2-yl)methyl] ethanethioate