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S-(4-fluorobutyl) ethanethioate

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Identification
Molecular formula
C6H11FO2S
CAS number
.
IUPAC name
S-(4-fluorobutyl) ethanethioate
State
State

At room temperature, S-(4-fluorobutyl) ethanethioate is a liquid, somewhat volatile, which should be handled with proper safety precautions to avoid inhalation or skin contact.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
170.00
Boiling point (Kelvin)
443.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2210g/mol
Density
1.0345g/cm3
Appearence

S-(4-fluorobutyl) ethanethioate is typically a colorless liquid. Depending on impurities or handling conditions, it may appear slightly yellowish.

Comment on solubility

Solubility of S-(4-fluorobutyl) ethanethioate

S-(4-fluorobutyl) ethanethioate is known for its unique chemical structure, which influences its solubility in various solvents. When assessing the solubility of this compound, consider the following key aspects:

  • Solvent Polarity: S-(4-fluorobutyl) ethanethioate is typically more soluble in polar solvents such as water or alcohols compared to nonpolar solvents. This is due to the presence of polar functional groups within its structure.
  • Temperature Effects: The solubility of this compound can significantly increase with rising temperature levels. A general rule of thumb is that higher temperatures often enhance the solubility of organic compounds.
  • Concentration Factors: Dilution plays a critical role; as the concentration of the solute increases, the solubility may reach a point of saturation, where further addition does not dissolve, leading to precipitate formation.
  • Comparison with Similar Compounds: When compared to other thioate esters, S-(4-fluorobutyl) ethanethioate may exhibit unique solubility characteristics due to the presence of the fluorobutyl group, which alters intermolecular forces and interactions in solution.

In summary, the solubility of S-(4-fluorobutyl) ethanethioate is intricately linked to factors such as solvent type, temperature, and concentration. Understanding these elements is crucial for applications where this compound is utilized. Always remember: "Solubility is a reflection of molecular interactions and the environment."

Interesting facts

Interesting Facts about S-(4-fluorobutyl) ethanethioate

S-(4-fluorobutyl) ethanethioate is a fascinating compound with several noteworthy characteristics. This compound features a unique combination of sulfur and fluorine, which leads to intriguing chemical behavior and potential applications.

Chemical Characteristics

  • Functional Group Diversity: The presence of both thioate and fluorobutyl groups in its structure makes this compound versatile for various reactions.
  • Potential Reactivity: The fluorine substituent enhances the electrophilicity of adjacent carbon atoms, potentially making it an interesting candidate for nucleophilic substitutions.

Applications in Research

  • As a Reagent: S-(4-fluorobutyl) ethanethioate can be used in organic synthesis to introduce sulfur-containing moieties in other compounds.
  • Biochemical Studies: Investigating the impact of fluorinated compounds on biological systems is crucial. This compound may spark research into its effects on enzyme activity or cellular interactions.

Quote from the Field

As noted by many researchers, “Fluorinated compounds often exhibit properties that are astonishingly different from their non-fluorinated counterparts.” This hints at the unique chemistry surrounding S-(4-fluorobutyl) ethanethioate.

Future Directions

The ongoing exploration of this compound offers potential breakthroughs in:

  • Material Science: Developing new materials with enhanced electrical properties.
  • Pharmaceutical Chemistry: Modifying drug designs to improve effectiveness and reduce side effects.

In conclusion, S-(4-fluorobutyl) ethanethioate is more than just a chemical name; it embodies a rich field of study with implications across various scientific disciplines.

Synonyms
4-Fluorobutyl thiolacetate
373-11-5
Butanethiol, 4-fluoro-, acetate
ACETIC ACID, THIO-, S-(4-FLUOROBUTYL) ESTER
BRN 1749682
Ethanethioic S-acid, 4-fluorobutyl ester
DTXSID50190743
4-02-00-00545 (Beilstein Handbook Reference)
SCHEMBL15402986
DTXCID90113234
YRZBWKXTJMKJIO-UHFFFAOYSA-N