6-amino-2-(p-tolylsulfonylamino)hexanamide
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- Molecular formula
- C13H20N2O3S
- CAS Number
- 15703-82-9
- IUPAC Name
- 6-amino-2-(p-tolylsulfonylamino)hexanamide
- Molecular Weight
- 285.39g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3036g/cm3
Identification
Interesting facts
Interesting Facts about 6-Amino-2-(p-tolylsulfonylamino)hexanamide
6-Amino-2-(p-tolylsulfonylamino)hexanamide is a fascinating compound with notable chemical properties and potential applications. Here are some intriguing aspects of this compound:
- Structural Features: This compound boasts a unique structure that includes an amino group and a sulfonamide moiety, which can play crucial roles in biological activity.
- Possible Therapeutic Uses: Sulfonamides are known for their antibacterial properties. Given its structure, 6-amino-2-(p-tolylsulfonylamino)hexanamide may exhibit similar antibacterial effects, making it a candidate for further research in medicinal chemistry.
- Importance in Drug Design: The presence of the p-tolylsulfonyl group could enhance the compound’s pharmacokinetic properties, such as solubility and bioavailability. This feature is essential in the design of effective pharmaceuticals.
- Versatility in Synthesis: The synthesis of this compound involves versatile reactions that can serve as a teaching point for students learning about organic synthesis methods, particularly in relation to amide formation and sulfonamide chemistry.
- Research Potential: Compounds with sulfonamide functionalities are actively researched for various applications, including their anti-inflammatory properties. This aspect opens up exciting possibilities for future studies on 6-amino-2-(p-tolylsulfonylamino)hexanamide.
As a compound that blends interesting structural elements with potential applications, 6-amino-2-(p-tolylsulfonylamino)hexanamide represents a captivating subject for both seasoned chemists and curious students alike. Exploring its properties could lead to significant discoveries in the fields of medicinal chemistry and organic synthesis.