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S-phenyl 2-fluoroethanethioate

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Identification
Molecular formula
C8H7FOS
CAS number
6938-18-7
IUPAC name
S-phenyl 2-fluoroethanethioate
State
State

At room temperature, S-phenyl 2-fluoroethanethioate is usually in a liquid state.

Melting point (Celsius)
-80.00
Melting point (Kelvin)
193.15
Boiling point (Celsius)
109.50
Boiling point (Kelvin)
382.65
General information
Molecular weight
184.22g/mol
Molar mass
184.2240g/mol
Density
1.1294g/cm3
Appearence

S-phenyl 2-fluoroethanethioate typically appears as a colorless to pale yellow liquid. Its appearance can vary slightly depending on purity and specific conditions.

Comment on solubility

Solubility of S-phenyl 2-fluoroethanethioate

S-phenyl 2-fluoroethanethioate, with the chemical formula C9H10F1OS, exhibits notable solubility characteristics that are important for its application in various chemical processes.

Generally, its solubility can be influenced by several factors, including:

  • Polarity: The presence of the fluorine functional group contributes to certain polar interactions, which can enhance solubility in polar solvents such as water and alcohols.
  • Temperature: As with many organic compounds, an increase in temperature can lead to improved solubility as molecular motion increases, allowing for better interaction with the solvent.
  • Solvent Choice: S-phenyl 2-fluoroethanethioate is more soluble in organic solvents, particularly non-polar and weakly polar solvents, such as hexane and ether.

In summary, while S-phenyl 2-fluoroethanethioate demonstrates moderate solubility in various solvents, it is essential to consider the specific conditions and solvent types to optimize its use in chemical reactions and applications. Experimenting with different solvent systems can help elucidate the most effective concentrations for practical uses.

Interesting facts

Interesting Facts about S-phenyl 2-fluoroethanethioate

S-phenyl 2-fluoroethanethioate is a fascinating compound that has garnered attention within the field of organic chemistry. Here are some intriguing aspects to consider:

  • Synthesis and Structure: This compound features a unique molecular structure, including a thioate functional group, which adds to its reactivity and potential applications in organic synthesis.
  • Chemical Properties: As a thioate, S-phenyl 2-fluoroethanethioate is known for its nucleophilic properties. The presence of the fluorine atom enhances its ability to participate in various chemical reactions, making it a valuable intermediate in the creation of more complex molecules.
  • Applications in Research: This compound is often utilized in academic and industrial research settings. Its functionality allows chemists to explore reaction mechanisms and develop new synthetic methods.
  • Biological Significance: There is ongoing research into the potential biological activities of S-phenyl 2-fluoroethanethioate. Compounds of similar structure have been known to exhibit antimicrobial and anticancer properties, making them subjects of interest in pharmacology.
  • Environmental Impact: Understanding the behavior of this compound in environmental contexts is essential. Its stability and reactivity can influence how it interacts with natural systems, leading to discussions about its ecological footprint.

In the words of a notable chemist, "The beauty of organic chemistry lies in its ability to transform the simplest building blocks into compounds with unexpected properties!" This rings true for S-phenyl 2-fluoroethanethioate, showcasing the creativity and innovation characteristic of the field.

As researchers continue to explore the depth of this compound, its relevance and application in modern chemistry are sure to grow, making it a topic worth following for anyone interested in the dynamic world of chemical compounds!

Synonyms
370-04-7
ACETIC ACID, FLUOROTHIO-, S-PHENYL ESTER
Phenyl fluorothiolacetate
BRN 3240822
17,846 RP
4-06-00-01523 (Beilstein Handbook Reference)
DTXSID30190488