3-(p-tolylsulfonyl)prop-2-enenitrile

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Identification

Molecular formula
C10H9NO2S
CAS Number
25186-60-5
IUPAC Name
3-(p-tolylsulfonyl)prop-2-enenitrile
Molecular Weight
205.26g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2340g/cm3
Synonyms
3-(p-Tolylsulfonyl)acrylonitrile
Interesting facts

Exploring 3-(p-tolylsulfonyl)prop-2-enenitrile

3-(p-tolylsulfonyl)prop-2-enenitrile is a fascinating compound that falls within the realm of organic chemistry. This compound is noteworthy for several reasons:

  • Versatility in Reactions: The presence of both the nitrile and sulfonyl functional groups makes this compound highly versatile and reactive, allowing it to participate in a variety of chemical reactions such as nucleophilic additions, condensation reactions, and more.
  • Applications: This compound can serve as a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. The sulfonyl group is often associated with compounds that exhibit biological activity, making it a significant focus in medicinal chemistry.
  • Impact on Drug Design: Designing drugs with sulfonamide or sulfonyl functionalities is a common strategy due to their roles in improving solubility and bioavailability. Compounds like 3-(p-tolylsulfonyl)prop-2-enenitrile, therefore, contribute directly to the development of new therapeutic agents.
  • Regioselectivity: The unique positioning of the functional groups in the structure allows for specific regioselectivity during chemical transformations, which can be a critical parameter in synthetic chemistry.

Overall, 3-(p-tolylsulfonyl)prop-2-enenitrile exemplifies the complexity and importance of organic compounds in the realm of chemical synthesis, drug design, and the development of innovative materials. Its study not only enhances our understanding of organic reactions but also bridges the gap between fundamental chemistry and practical applications.

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