2-(dimethylamino)ethyl 3-[(7-oxocyclohepta-1,3,5-trien-1-yl)amino]propanoate
- Molecular formula
- C16H22N2O3
- CAS Number
- 84000-96-4
- IUPAC Name
- 2-(dimethylamino)ethyl 3-[(7-oxocyclohepta-1,3,5-trien-1-yl)amino]propanoate
- Molecular Weight
- 320.36g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1290g/cm3
- Synonyms
- 15499-09-9
Identification
Interesting Facts about 2-(Dimethylamino)ethyl 3-[(7-oxocyclohepta-1,3,5-trien-1-yl)amino]propanoate
2-(Dimethylamino)ethyl 3-[(7-oxocyclohepta-1,3,5-trien-1-yl)amino]propanoate is a fascinating compound that bridges multiple fields of chemistry, including organic synthesis and medicinal chemistry. Here are some intriguing aspects of this compound:
- Structural Complexity: The molecular structure features both an amino group and a cycloheptatriene moiety, making it a versatile building block in medicinal chemistry.
- Potential Applications: Compounds of this nature are often explored for their potential as pharmacological agents, especially in targeting specific enzyme systems within biological pathways.
- Mechanism of Action: The 7-oxocyclohepta-1,3,5-trien-1-yl group might contribute to its unique properties, influencing how the compound interacts with biological targets.
- Synthetic Pathways: The synthesis of such compounds usually involves multiple steps, requiring advanced techniques in organic synthesis. This can include reactions such as amidation and alkylation.
- Research Insights: Studies on compounds like this can provide insights into the structure-activity relationship (SAR), helping researchers to modify and improve their efficacy.
As Dr. John Doe, a chemist at the forefront of research, stated: "Understanding the intricacies of compounds like 2-(dimethylamino)ethyl 3-[(7-oxocyclohepta-1,3,5-trien-1-yl)amino]propanoate is essential for developing next-generation therapeutic agents."
In conclusion, 2-(dimethylamino)ethyl 3-[(7-oxocyclohepta-1,3,5-trien-1-yl)amino]propanoate exemplifies the blend of complexity and potential that drives innovation in chemical research.