S-(chloromethyl) ethanethioate

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Identification

Molecular formula
C3H5ClOS
CAS Number
19720-58-8
IUPAC Name
S-(chloromethyl) ethanethioate
Molecular Weight
124.60g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2623g/cm3
Synonyms
SCHEMBL10660909
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.

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