N-(2-aminoethyl)-4-chloro-benzamide
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- Molecular formula
- C9H11ClN2O
- CAS Number
- 121-56-8
- IUPAC Name
- N-(2-aminoethyl)-4-chloro-benzamide
- Molecular Weight
- 200.65g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2960g/cm3
- Synonyms
- N-(2-aminoethyl)-4-chlorobenzamide
Identification
Interesting facts
Interesting Facts about N-(2-Aminoethyl)-4-chloro-benzamide
N-(2-aminoethyl)-4-chloro-benzamide is a fascinating compound that finds its applications in the fields of medicinal chemistry and organic synthesis. Here are some intriguing aspects of this compound:
- Pharmaceutical Relevance: This compound is often studied for its potential role in drug development, particularly as a scaffold for creating various pharmaceutical agents.
- Biological Activity: N-(2-aminoethyl)-4-chloro-benzamide may exhibit significant interaction with biological targets, making it a candidate for further investigation in the realm of biological sciences.
- Synthesis Challenge: Its synthesis can be quite challenging, often requiring careful consideration of reaction conditions and reagent selection, providing a valuable learning experience for budding chemists.
- Applications in Research: This compound is often utilized in research to explore the structure-activity relationships of similar chemical entities, broadening the understanding of how different functional groups affect the properties of compounds.
- Multi-Functional Potential: Due to the presence of both amine and amide functional groups, N-(2-aminoethyl)-4-chloro-benzamide can serve as a versatile intermediate in organic transformations.
The study of compounds like N-(2-aminoethyl)-4-chloro-benzamide not only enhances our understanding of chemistry but also paves the way for future innovations in pharmaceuticals and materials science. As a quote by renowned chemist Robert H. Grubbs states, "Chemistry is the science of matter, but I prefer to see it as the science of change." In this case, the study of such compounds exemplifies the transformative nature of chemical research.