Ethyl 3-(2-sulfamoylphenyl)prop-2-enoate
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- Molecular formula
- C11H13NO4S
- CAS Number
- 915783-27-4
- IUPAC Name
- ethyl 3-(2-sulfamoylphenyl)prop-2-enoate
- Molecular Weight
- 265.28g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3122g/cm3
Identification
Interesting facts
Interesting Facts About Ethyl 3-(2-Sulfamoylphenyl)prop-2-enoate
Ethyl 3-(2-sulfamoylphenyl)prop-2-enoate is a compound that captivates the interest of chemists due to its unique structural features and potential applications. Here are some noteworthy aspects to consider:
- Sulfamoyl Group: The presence of the sulfamoyl group (-SO2NH2) is particularly intriguing, as it is associated with a variety of biological activities. Compounds containing this group have been studied for their antimicrobial properties.
- Biological Significance: Research has indicated that derivatives of sulfonamides, which include the sulfamoyl moiety, demonstrate significant efficacy in medicinal chemistry, particularly in developing drugs to combat bacterial infections.
- Versatile Functionality: The ethyl ester component provides versatility in synthetic chemistry, allowing for various modifications that can enhance its properties or create novel compounds.
- Potential for Drug Development: Researchers are continuously looking at compounds like ethyl 3-(2-sulfamoylphenyl)prop-2-enoate for their potential as lead structures in drug design.
The structure of this compound is also notable for its geometric isomerism, highlighting the importance of stereochemistry in determining chemical reactivity and biological activity.
In summary, this compound is not just a chemical entity; it represents a bridge between synthetic organic chemistry and potential therapeutic applications, making it a compelling topic for further exploration.