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S-(2-Fluoroethyl) ethanethioate

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Identification
Molecular formula
C4H7FO1S1
CAS number
383-63-1
IUPAC name
S-(2-fluoroethyl) ethanethioate
State
State

At room temperature, S-(2-Fluoroethyl) ethanethioate is typically in a liquid state.

Melting point (Celsius)
-70.50
Melting point (Kelvin)
202.65
Boiling point (Celsius)
146.00
Boiling point (Kelvin)
419.15
General information
Molecular weight
122.18g/mol
Molar mass
122.1760g/mol
Density
1.1564g/cm3
Appearence

S-(2-Fluoroethyl) ethanethioate is typically a colorless liquid. Its appearance is clear, and it has a characteristic odor associated with thiol esters.

Comment on solubility

Solubility of S-(2-fluoroethyl) ethanethioate

The solubility of S-(2-fluoroethyl) ethanethioate presents intriguing characteristics that are worth examining. This compound demonstrates varying solubility behaviors in different solvents, primarily influenced by its molecular structure and functional groups. Here are some key points regarding its solubility:

  • Polar Solvents: Due to the presence of the thioate functional group, S-(2-fluoroethyl) ethanethioate tends to have better solubility in polar solvents such as water and alcohols. The polarity of these solvents can stabilize the compound through hydrogen bonding.
  • Non-Polar Solvents: Conversely, the compound may show limited solubility in non-polar solvents like hexane or benzene. This is attributed to its polar characteristics which favor interactions with polar rather than non-polar environments.
  • Temperature Dependency: The solubility is also temperature-dependent, indicating that increased temperatures may enhance solubility by providing sufficient energy to overcome intermolecular forces and facilitate dissolution.

In summary, one might conclude that the solubility of S-(2-fluoroethyl) ethanethioate is multifaceted, impacted by various factors including solvent polarity, temperature, and the unique properties of its molecular structure. As the saying goes, "like dissolves like," hence understanding these characteristics is essential for predicting its behavior in different chemical environments.

Interesting facts

Interesting Facts About S-(2-fluoroethyl) ethanethioate

S-(2-fluoroethyl) ethanethioate is a fascinating compound, particularly noteworthy for its unique structure and potential applications. Here are some interesting insights:

  • Composition: This compound consists of a thioester, a functional group derived from the reaction between a carboxylic acid and a thiol. The presence of a fluoroethyl group greatly influences its chemical behavior and reactivity.
  • Biological Activity: Compounds containing fluorine have been extensively studied due to their enhanced biological activity. The fluorine substituent can improve the lipophilicity of molecules, allowing them to better penetrate biological membranes.
  • Applications in Agrochemicals: S-(2-fluoroethyl) ethanethioate may find potential use in the development of agrochemicals. The modification of existing thioester compounds with fluorinated groups can lead to improved pesticides or herbicides, which may possess greater efficacy or reduced toxicity.
  • Reactivity: The presence of the thioester moiety also makes this compound interesting for various organic synthesis reactions. Thioesters can be hydrolyzed, exchanged, or converted into other functional groups, making them versatile intermediates in synthetic chemistry.
  • Innovation in Pharmaceuticals: Fluorinated compounds are increasingly utilized in pharmaceuticals due to their ability to enhance metabolic stability and modify biological responses, potentially leading to improved therapeutic agents.

Overall, S-(2-fluoroethyl) ethanethioate exemplifies the intersection of innovation and chemistry, showcasing how small changes in molecular structure can lead to significant implications in various scientific fields. The exploration of such compounds will undoubtedly continue to inspire chemists in their pursuit of discovery.

Synonyms
462-31-7
ACETIC ACID, THIO-, S-(2-FLUOROETHYL) ESTER
2-Fluoroethyl thiolacetate
BRN 1743106
Ethanethioic S-acid, 2-fluoroethyl ester
4-02-00-00544 (Beilstein Handbook Reference)
SCHEMBL16352674
DTXSID10196761
thioacetic acid, 2-fluoroethyl ester