N,N-dimethyl-N'-(1-phenylethyl)formamidine
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- Molecular formula
- C11H16N2
- CAS Number
- 2486-26-4
- IUPAC Name
- N,N-dimethyl-N'-(1-phenylethyl)formamidine
- Molecular Weight
- 176.26g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0540g/cm3
- Synonyms
- BRN 2830533
Identification
Interesting facts
Interesting Facts About N,N-Dimethyl-N'-(1-phenylethyl)formamidine
N,N-Dimethyl-N'-(1-phenylethyl)formamidine is a remarkable compound known for its unique structure and various applications in the field of chemistry. Here are some fascinating insights:
- Versatile Intermediate: This compound serves as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure allows for modifications that can lead to a variety of active compounds.
- Mechanism of Action: Researchers have observed that compounds similar to N,N-dimethyl-N'-(1-phenylethyl)formamidine often mimic biological activity due to their ability to interact with specific biological receptors. This opens doors for potentially new therapeutic agents.
- Research Applications: It has been explored in research involving enzyme inhibition and biological assays, showcasing its relevance in medicinal chemistry and drug development.
- Synthesis Approach: The synthesis of this compound involves a series of reactions that typically include condensation reactions, demonstrating the principles of organic chemistry and functional group transformations.
- Structure-Activity Relationship (SAR): Investigating the SAR of this compound can yield insights into how structural changes affect its biological activity, making it a valuable topic of study for chemists looking to optimize drug design.
In sum, N,N-dimethyl-N'-(1-phenylethyl)formamidine is not just an ordinary compound but a gateway to understanding complex chemical interactions and developing innovative solutions in medicine and agriculture. Its continued study could lead to groundbreaking discoveries in organic synthesis and pharmacology.