3-(Benzenesulfonyl)-1-phenylisothiourea
- Molecular formula
- C13H12N2O2S2
- CAS Number
- 57045-64-6
- IUPAC Name
- 3-(benzenesulfonyl)-1-phenyl-isothiourea
- Molecular Weight
- 274.37g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3400g/cm3
Identification
Interesting Facts about 3-(Benzenesulfonyl)-1-phenyl-isothiourea
3-(Benzenesulfonyl)-1-phenyl-isothiourea is a fascinating compound notable for its diverse applications and unique structural characteristics. Here are some captivating aspects:
- Structural Features: This compound contains an isothiourea moiety, which is often characterized by a sulfur atom bonded to both a nitrogen atom and a carbon atom, giving it distinct chemical properties.
- Biological Relevance: Compounds like 3-(benzenesulfonyl)-1-phenyl-isothiourea have been studied for their potential biological activities. They display interesting pharmacological profiles which may contribute to therapeutic applications.
- Synthesis: The synthesis of this compound can involve methods that typically incorporate sulfonation reactions, making it a good example for students learning organic synthesis techniques.
- Research Applications: This compound has gained attention in chemical research, particularly in the study of enzyme inhibitors, which are crucial in drug development processes.
A notable quote from a renowned chemist reminds us of the importance of functionalized thioureas in organic chemistry: "The versatility of thiourea derivatives in various chemical transformations is truly remarkable." As we explore the world of isothioureas, compounds like 3-(benzenesulfonyl)-1-phenyl-isothiourea exemplify the intricate connections between structure and function in chemical compounds.
In summary, the exploration of this compound not only enriches our understanding of organic chemistry but also highlights the potential implications in medicinal chemistry and drug design.