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S-(chloromethyl) ethanethioate

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Identification
Molecular formula
C3H5ClOS
CAS number
19720-58-8
IUPAC name
S-(chloromethyl) ethanethioate
State
State

At room temperature, S-(chloromethyl) ethanethioate is a liquid. It is volatile with the potential to evaporate at mildly elevated temperatures.

Melting point (Celsius)
-52.00
Melting point (Kelvin)
221.15
Boiling point (Celsius)
126.00
Boiling point (Kelvin)
399.15
General information
Molecular weight
124.60g/mol
Molar mass
124.6040g/mol
Density
1.2623g/cm3
Appearence

S-(chloromethyl) ethanethioate is a colorless to light yellow liquid with a distinctive odor. The substance has an oily texture and is typically transparent, though impurities can give it a slight opalescence.

Comment on solubility

Solubility of S-(chloromethyl) ethanethioate

S-(chloromethyl) ethanethioate, with its unique structure, presents interesting solubility characteristics that are vital for various applications. Its solubility can be influenced by several factors:

  • Polarity: This compound contains both a chloromethyl group and a thioate group, which can enhance its polarity. Polarity often correlates with solubility in polar solvents, such as water.
  • Hydrophobic Interactions: The presence of the ethyl group can induce some hydrophobic behavior, potentially reducing solubility in aqueous environments.
  • Temperature: As with many chemical compounds, temperature can significantly affect solubility. Increased temperatures may enhance solubility through thermal agitation, providing more energy for the dissolution process.
  • Concentration: The concentration of the solution can also play a role. Higher concentrations may lead to saturation, affecting the overall solubility dynamics.

In essence, while S-(chloromethyl) ethanethioate may demonstrate limited solubility in water due to its structural features, it may find better solubility in organic solvents. As a researcher or chemist, it's crucial to experiment with various solvents and conditions to determine the precise solubility profile of this intriguing compound.

Interesting facts

Exploring S-(Chloromethyl) Ethanethioate

S-(Chloromethyl) ethanethioate is a fascinating compound noteworthy for its diverse applications in the realm of organic chemistry and material sciences. Here are some captivating insights:

  • Reactivity: This compound serves as an important intermediate in the synthesis of various other chemicals. Its chloromethyl group provides a reactive site for nucleophilic substitution reactions, making it a valuable building block.
  • Biological Significance: Some derivatives of S-(chloromethyl) ethanethioate have been studied for their potential biological activity, particularly in drug development, exploring their impact on certain biochemical pathways.
  • Versatile Applications: This compound is utilized in the manufacture of pesticides and herbicides, showcasing its role in agriculture by improving crop yields while addressing pest control.
  • Environmental Factors: While this compound has significant industrial utility, its environmental persistence raises concerns that prompt ongoing research into safer alternatives.
  • Structural Insights: The unique structure of S-(chloromethyl) ethanethioate affords interesting physical and chemical properties, making it a subject of study for chemists interested in sulfur-containing compounds.

In summary, S-(chloromethyl) ethanethioate represents a compelling intersection of chemistry with real-world applications, bridging the gap between laboratory research and practical use in numerous sectors. As a chemist, one might find the exploration of its properties and reactions not only intellectually stimulating but also crucial for innovation.

Synonyms
SCHEMBL10660909
AKOS006383606