sec-butyl 3-(2-sulfamoylphenyl)prop-2-enoate

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Identification

Molecular formula
C13H17NO4S
CAS Number
85263-32-1
IUPAC Name
sec-butyl 3-(2-sulfamoylphenyl)prop-2-enoate
Molecular Weight
270.35g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2500g/cm3
Interesting facts

Interesting Facts about sec-butyl 3-(2-sulfamoylphenyl)prop-2-enoate

sec-butyl 3-(2-sulfamoylphenyl)prop-2-enoate is an intriguing compound that has drawn attention for its potential applications in medicinal chemistry. This compound features a unique structure that incorporates a sulfamoyl group, which significantly enhances its biological activity. Here are some fascinating details:

  • Pharmaceutical Potential: The incorporation of the sulfonamide group in the structure makes this compound a candidate for anti-inflammatory and antimicrobial properties. The sulfamoyl moiety is known for its role in various drug actions.
  • Synthesis Approaches: The synthesis of this compound often involves Michael addition reactions, providing a valuable example of how functional groups can be effectively introduced into organic frameworks.
  • Importance in Drug Design: Compounds like sec-butyl 3-(2-sulfamoylphenyl)prop-2-enoate serve as pivotal platforms in the design of more complex pharmaceuticals, showcasing how small modifications can lead to varying biological effects.
  • Structure-Activity Relationship (SAR): Investigating SAR can illuminate how the presence of the sulfamoyl group influences pharmacodynamics and pharmacokinetics, vital for optimizing therapeutic efficacy.

The study of sec-butyl 3-(2-sulfamoylphenyl)prop-2-enoate exemplifies the dynamic nature of organic chemistry and its capacity to innovate in drug development. It's a testament to how a seemingly simple molecule can harbor complex interactions within biological systems, paving the way for future research and therapeutic breakthroughs.

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