4-(4-chlorophenyl)thio-1-butanol

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Identification

Molecular formula
C10H13ClOS
CAS Number
94413-64-2
IUPAC Name
4-(4-chlorophenyl)sulfanylbutan-1-ol
Molecular Weight
216.72g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2000g/cm3
Appearance
may vary slightly depending on the form of the sample and its purity, but it is generally a solid at room temperature.
Synonyms
4-(p-Chlorophenylthio)butanol
Interesting facts

Interesting Facts about 4-(4-chlorophenyl)sulfanylbutan-1-ol

4-(4-chlorophenyl)sulfanylbutan-1-ol is a fascinating compound that belongs to the family of organosulfur compounds. Its structure encompasses a butanol backbone which is substituted with both a chlorophenyl group and a sulfanyl group, imparting unique properties and interactions. Here are some interesting aspects to consider:

  • Biological Relevance: This compound is of interest in medicinal chemistry due to its potential biological activities. Sulfur-containing compounds often exhibit a range of pharmacological properties, making them candidates for further research in drug development.
  • Structure-Activity Relationship: The presence of the chlorophenyl moiety significantly affects the chemical reactivity and biological activity of this compound. Investigating how these modifications influence the molecular properties can provide insights into the design of more effective therapeutic agents.
  • Reaction Pathways: Compounds like 4-(4-chlorophenyl)sulfanylbutan-1-ol can participate in various chemical reactions, including nucleophilic substitution and oxidation reactions, which are vital for synthetic organic chemistry.
  • Industrial Applications: Organosulfur compounds are widely used in several industries, including agrochemicals, pharmaceuticals, and materials science. Their versatility has sparked interest in applications ranging from pest control to advanced materials development.
  • Synthetic Pathways: Researchers often explore different synthetic routes to produce such compounds. This includes the use of thiol and halide-based reagents, allowing for diverse methodological approaches in laboratory settings.

In summary, 4-(4-chlorophenyl)sulfanylbutan-1-ol showcases the rich interplay of structure and function in organic chemistry. Its unique characteristics and potentials make it a significant subject for further research and exploration in various scientific fields.

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