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2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate

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Identification
Molecular formula
C14H20FO4PS
CAS number
64162-83-0
IUPAC name
2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate
State
State
The compound is typically a liquid at room temperature. It shows low volatility and does not solidify under standard atmospheric conditions.
Melting point (Celsius)
0.00
Melting point (Kelvin)
273.15
Boiling point (Celsius)
315.20
Boiling point (Kelvin)
588.35
General information
Molecular weight
360.35g/mol
Molar mass
360.4250g/mol
Density
1.1945g/cm3
Appearence

2-Fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate is a clear to pale yellow liquid. It might have a characteristic odor depending on the synthesis process. No solid form is typically noted under normal conditions.

Comment on solubility

Solubility of 2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate

The solubility of the compound 2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate can be influenced by several factors including its molecular structure and functional groups present.

Generally, the solubility characteristics can be summarized as follows:

  • Polarity: The presence of the diethoxy group as well as the phosphinothioyl and sulfanyl functionalities contribute to the overall polarity of the compound, which may enhance its solubility in polar solvents.
  • Hydrophobic Interactions: The phenyl group could introduce hydrophobic interactions, making the compound less soluble in water but possibly more soluble in organic solvents such as ethanol or ether.
  • Temperature Dependence: Solubility can vary with temperature; generally, solubility increases as temperature rises for many compounds. This compound may exhibit similar behavior.
  • pH Sensitivity: If the compound has protonatable functional groups, its solubility might change with varying pH, particularly in aqueous solutions.

In practical applications, when considering the usage of 2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate, it is essential to experiment with different solvents and conditions for optimal solubility results. As with many compounds in this realm, it is crucial to say that “solubility is not just a property but a pathway to functionality.” Thus, understanding these factors can lead to better utilization in chemical processes.

Interesting facts

Interesting Facts about 2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate

The compound 2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenyl-acetate exhibits some fascinating properties and applications that are noteworthy for both chemists and students alike. It belongs to the class of organophosphorus compounds, which are of particular interest due to their diverse roles in various fields.

Key Features:

  • Biological Activity: This compound is explored for its potential in the field of agrochemicals, specifically as a pesticide or herbicide. Its organophosphorus framework allows it to interact effectively with biological systems, making it a candidate for further research into sustainable pest management.
  • Fluorine Substitution: The presence of the fluoroethyl group can enhance the lipophilicity of the compound, which might optimize its biological uptake and efficacy. This introduces interesting avenues in medicinal chemistry, where fluorinated compounds are often more bioactive.
  • Phosphinothioyl Functionality: The phosphinothioyl moiety in the structure contributes to the compound’s unique reaction pathways, potentially leading to innovative methods in synthetic routes or catalysis.

Moreover, the incorporation of distinct functional groups in the molecular structure fosters a wide range of chemical reactivity, lending itself to potential cross-coupling reactions and other synthetic applications. As one researcher articulates, “The interplay of phosphorous and sulfur within organophosphorus chemistry opens doors to unexplored territories in synthesis and material science.”

This compound, while complex, epitomizes the intricate nature of organophosphorus compounds. Its study not only expands our understanding of chemical interactions but also bridges gaps between organic chemistry and applied fields such as agriculture and pharmaceuticals.

Synonyms
4681-36-1
Acetic acid, mercaptophenyl-, 2-fluoroethyl ester, S-ester with O,O-diethyl phosphorodithioate
M 1788
2-Fluoroethyl mercaptophenylacetate, O,O-diethyl phosphorodithioate
Fluoroethyl O,O-diethyldithiophosphoryl-1-phenylacetate
2-fluoroethyl 2-diethoxyphosphinothioylsulfanyl-2-phenylacetate
2-Fluoroethyl 2-((diethoxyphosphorothioyl)thio)-2-phenylacetate
starbld0023022
DTXSID50963671
AKOS040750084
2-fluoroethyl [(diethoxyphosphorothioyl)sulfanyl](phenyl)acetate