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Furadan

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Identification
Molecular formula
C8H9N3O6
CAS number
4774-14-5
IUPAC name
2-hydroxyethyl N-[(5-nitro-2-furyl)methyleneamino]carbamate
State
State

At room temperature, the compound is usually found as a crystalline solid.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.15
General information
Molecular weight
243.17g/mol
Molar mass
243.1900g/mol
Density
1.4740g/cm3
Appearence

The compound typically appears as a yellow to orange crystalline solid.

Comment on solubility

Solubility of 2-hydroxyethyl N-[(5-nitro-2-furyl)methyleneamino]carbamate

The solubility of 2-hydroxyethyl N-[(5-nitro-2-furyl)methyleneamino]carbamate can be influenced by several factors due to its complex structure. Here are some key points to consider:

  • Solvent Compatibility: This compound is expected to exhibit varying solubility in polar and non-polar solvents. Generally, such carbamates are more soluble in polar solvents due to their hydrogen bonding capabilities.
  • pH Sensitivity: The solubility can significantly change with pH adjustments. It may become more soluble in alkaline conditions where deprotonation occurs.
  • Temperature Dependency: Like many chemical compounds, solubility often increases with temperature. Thus, elevated temperatures may enhance the dissolution process.
  • Concentration Effects: Increased concentrations can lead to saturation limits being reached, which should be considered in applications.

In conclusion, the solubility of this compound is a multifaceted issue, dependent on the surrounding environment. For researchers and practitioners, understanding these variables is crucial for optimizing the use of 2-hydroxyethyl N-[(5-nitro-2-furyl)methyleneamino]carbamate in various applications. As with many compounds, precise solubility measurements should be conducted under specific conditions for accurate data.

Interesting facts

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.