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2-(2-Nitrovinyl)furan

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Identification
Molecular formula
C6H5NO3
CAS number
10315-77-2
IUPAC name
2-(2-nitrovinyl)furan
State
State

At room temperature, 2-(2-Nitrovinyl)furan is in a solid state.

Melting point (Celsius)
54.00
Melting point (Kelvin)
327.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
151.11g/mol
Molar mass
151.1310g/mol
Density
1.2700g/cm3
Appearence

2-(2-Nitrovinyl)furan appears as a yellow to orange crystalline solid. It can exhibit some degree of light sensitivity, potentially changing color slightly when exposed to light over time.

Comment on solubility

Solubility of 2-(2-nitrovinyl)furan

2-(2-nitrovinyl)furan, a compound with both nitro and furan functional groups, exhibits intriguing solubility characteristics. Its solubility behavior is influenced by several factors that include:

  • Polarity: The presence of nitro groups significantly enhances polarity, which can affect its solubility in polar solvents.
  • Hydrogen Bonding: The furan ring can participate in hydrogen bonding, potentially increasing solubility in protic solvents.
  • Solvent Interaction: It tends to dissolve better in organic solvents such as ethanol and acetone compared to water due to its organic nature.

Typically, it is said that "like dissolves like"; thus, 2-(2-nitrovinyl)furan is more likely to dissolve efficiently in non-polar or slightly polar organic solvents than in highly polar solvents. Experimentally determined solubility data indicates that its solubility can vary widely depending on the environmental conditions, such as temperature and the presence of other solutes. As an interesting aspect of this compound, its solubility can also be a critical factor in assessing its reactivity and potential applications in various chemical processes.

Interesting facts

Interesting Facts about 2-(2-Nitrovinyl)furan

2-(2-Nitrovinyl)furan is an intriguing chemical compound that has garnered attention in the fields of organic chemistry and materials science. Here are some fascinating aspects of this compound:

  • Unique Structure: The structure of 2-(2-nitrovinyl)furan features a furan ring, which is a five-membered aromatic ring containing oxygen. The presence of the nitrovinyl group adds a level of complexity and enhances its reactivity.
  • Potential Applications: This compound is studied for its potential in various applications, including:
    • Organic synthesis: It can serve as a building block for the synthesis of more complex molecules.
    • Material science: Its reactive nature allows it to be used in the development of novel materials with desirable properties.
  • Electron-Withdrawing Properties: The nitro group in the molecule is a strong electron-withdrawing group. This characteristic influences the chemical reactivity of the compound, making it a valuable tool in electrophilic aromatic substitution reactions.
  • Research Interest: Studies involving 2-(2-nitrovinyl)furan have provided insights into reaction mechanisms and the development of new synthetic pathways. Researchers continue to explore its properties, leading to potential breakthroughs in drug development and other chemical innovations.

In conclusion, the study of 2-(2-nitrovinyl)furan not only helps deepen our understanding of organic chemistry but also opens doors to the design of innovative applications and materials.

Synonyms
Furan, 2-[(1E)-2-nitroethenyl]-
2-(B-nitrovinyl)furan
2-[(1E)-2-nitroethenyl]furan
nitrovinylfuran
2-(2-nitrovinyl)-furan
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HBA78245
AKOS030230563
SB61076
SY076936
DB-018435