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Ethyl 3-(5-nitro-2-furyl)acrylate

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Identification
Molecular formula
C9H7NO5
CAS number
5871-12-1
IUPAC name
ethyl 3-(5-nitro-2-furyl)prop-2-enoate
State
State

At room temperature, ethyl 3-(5-nitro-2-furyl)acrylate is found in a solid crystalline state. It is known for being relatively stable under standard laboratory conditions but, like many nitro compounds, should be handled with care to avoid exposure to heat or sparks.

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.15
Boiling point (Celsius)
383.00
Boiling point (Kelvin)
656.15
General information
Molecular weight
225.16g/mol
Molar mass
225.1840g/mol
Density
1.2885g/cm3
Appearence

Ethyl 3-(5-nitro-2-furyl)acrylate is typically a yellow to orange crystalline solid. Its vivid coloration is attributed to the presence of the nitrofuran group in the structure. It is often synthesized and handled in its solid form.

Comment on solubility

Solubility of Ethyl 3-(5-nitro-2-furyl)prop-2-enoate

Ethyl 3-(5-nitro-2-furyl)prop-2-enoate, a compound featuring both aromatic and aliphatic characteristics, has a solubility profile that can be quite intriguing. Here are some key points regarding its solubility:

  • Polar vs. Non-Polar: Due to the presence of the nitro group and the ester functional group, this compound exhibits a balance of polarity, which allows it to interact well with various solvents.
  • Solvent Compatibility: It is generally more soluble in polar organic solvents such as ethanol and methanol, compared to non-polar solvents. The ability to dissolve in polar solvents is primarily influenced by hydrogen bonding capabilities.
  • Water Solubility: The solubility of this compound in water is likely limited. While some functional groups can enhance solubility in water, the overall structure tends to favor organic phases.
  • Temperature Effect: Like many organic compounds, its solubility may increase with temperature, making hot solvents potentially useful for dissolution.

In conclusion, understanding the solubility of ethyl 3-(5-nitro-2-furyl)prop-2-enoate not only facilitates its practical applications in organic synthesis but also unveils intriguing possibilities for its behavior in various environments. Analyzing how functional groups influence solubility can provide insight into predicting the behavior of similar compounds in chemical contexts.

Interesting facts

Interesting Facts About Ethyl 3-(5-nitro-2-furyl)prop-2-enoate

Ethyl 3-(5-nitro-2-furyl)prop-2-enoate is a fascinating compound that falls into the category of nitrofuran derivatives. These compounds have garnered significant interest in the scientific community due to their various applications and unique properties. Here are some intriguing details about this compound:

  • Nitro Group Influence: The presence of the nitro group (-NO2) in the structure plays a crucial role in the reactivity and biological activity of this compound, making it an interesting subject for medicinal chemistry.
  • Furan Ring Significance: The furan ring is a five-membered aromatic ring containing oxygen. Compounds with furan moieties are often explored for their potential as antioxidants and anti-inflammatory agents.
  • Potential Applications: Due to its structural characteristics, ethyl 3-(5-nitro-2-furyl)prop-2-enoate may have applications in pharmaceuticals, particularly in the development of new drugs that target cancer or microbial infections.
  • Chemoselectivity: The unique combination of a furan ring and a nitro group can lead to interesting chemoselective reactions. Understanding these reactions can be critical for synthetic chemists.
  • Research Interest: This compound is part of ongoing research aimed at exploring the synthesis of new materials and their biological activities, making it a target for both organic chemists and biochemists.

As we dive deeper into the world of organic compounds, exploring the properties and potentials of chemicals like ethyl 3-(5-nitro-2-furyl)prop-2-enoate enhances our understanding of materials science and drug development. The exploration of its various properties could very well pave the way for innovative therapeutic strategies.

Synonyms
ethyl 3-(5-nitrofuran-2-yl)prop-2-enoate
2-Propenoic acid, 3-(5-nitro-2-furanyl)-, ethyl ester, (E)-
2-Propenoic acid, 3-(5-nitro-2-furanyl)-, ethyl ester
DTXSID0075150