Disopyramide
- Molecular formula
- C21H29N3O3
- CAS Number
- 3737-09-5
- IUPAC Name
- 2-[2-(ethylcarbamoyloxy)ethyl-methyl-amino]ethyl N-ethylcarbamate
- Molecular Weight
- 339.48g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1630g/cm3
Identification
Interesting Facts about 2-[2-(ethylcarbamoyloxy)ethyl-methyl-amino]ethyl N-ethylcarbamate
2-[2-(ethylcarbamoyloxy)ethyl-methyl-amino]ethyl N-ethylcarbamate is a fascinating compound with a diverse range of applications and properties. Here are some intriguing facts that highlight its significance:
- Dual Utility: This compound serves a dual purpose; being utilized both in pharmaceuticals and agrochemicals, it showcases versatility in its applications.
- Structural Complexity: The complex structure of this compound, featuring multiple functional groups, makes it a subject of interest in organic synthesis and medicinal chemistry.
- Bioactivity: Compounds with carbamate linkages often exhibit interesting biological activities, including potential pest control properties, which emphasize their utility in both health and agriculture.
- Research Potential: The intricate nature of 2-[2-(ethylcarbamoyloxy)ethyl-methyl-amino]ethyl N-ethylcarbamate opens avenues for various research studies, focusing on drug design and discovery.
- Reactant in Multi-Step Synthesis: This compound can serve as a key reactant in multi-step organic synthesis, allowing chemists to build complex structures necessary for developing novel therapeutic agents.
As a scientist studying this compound, one might reflect on how "**every new compound opens doors to endless possibilities**" in fields ranging from medicinal chemistry to environmental science. The **interplay of its chemical properties** not only aids in innovation but also poses challenges related to stability, reactivity, and bioactivity.
In summary, the exploration of 2-[2-(ethylcarbamoyloxy)ethyl-methyl-amino]ethyl N-ethylcarbamate provides a captivating glimpse into the intersection of chemistry, biology, and practical application.