Furadan
- Molecular formula
- C8H9N3O6
- CAS Number
- 4774-14-5
- IUPAC Name
- 2-hydroxyethyl N-[(5-nitro-2-furyl)methyleneamino]carbamate
- Molecular Weight
- 243.17g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4740g/cm3
Identification
Interesting Facts about 2-Hydroxyethyl N-[(5-Nitro-2-Furyl)methyleneamino]carbamate
This fascinating compound is a member of the carbamate family, and it showcases versatile applications in various fields, particularly in medicinal chemistry and agriculture. Its structure features a unique 5-nitro-2-furyl moiety, which significantly contributes to its biological activity.
Biological Significance
2-Hydroxyethyl N-[(5-nitro-2-furyl)methyleneamino]carbamate has garnered attention due to its potential therapeutic properties:
- Antimicrobial Activity: The nitro group in the furan ring is known for enhancing the compound's ability to combat microbial infections.
- Potential Antitumor Effects: Studies suggest that this compound may inhibit cancer cell proliferation, making it a candidate for further research in oncology.
- Enzymatic Inhibition: Its carbamate functionality allows for interactions with certain enzymes, potentially serving as an inhibitor in biochemical pathways.
Chemical Structure and Properties
The compound's structure includes:
- A hydroxyl group that increases its solubility in biological systems.
- A furan ring that introduces heterocyclic features, influencing the compound's reactivity and interaction with biological macromolecules.
- The carbamate group that is critical for its biological activity and stability.
As a scientist, one can appreciate how the intricate design of such compounds can lead to numerous applications. The synergistic effects of the different functional groups present in this molecule allow it to interact with various biological targets. This complexity is what makes the study of such compounds both challenging and rewarding.
In conclusion, 2-hydroxyethyl N-[(5-nitro-2-furyl)methyleneamino]carbamate serves as a remarkable example of how the interplay of organic functional groups can create compounds with significant potential in both research and therapeutic contexts.