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2-nitronon-2-ene

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Identification
Molecular formula
C9H17NO2
CAS number
105614-55-1
IUPAC name
2-nitronon-2-ene
State
State

At room temperature, 2-nitronon-2-ene is a liquid.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.15
Boiling point (Celsius)
232.40
Boiling point (Kelvin)
505.55
General information
Molecular weight
157.21g/mol
Molar mass
157.2090g/mol
Density
0.9275g/cm3
Appearence

2-Nitronon-2-ene is a liquid with a pale yellow color. It typically has a strong, pungent odor characteristic of nitroalkenes.

Comment on solubility

Solubility of 2-nitronon-2-ene

2-nitronon-2-ene, with the chemical formula C9H13NO2, exhibits moderate solubility properties primarily due to its molecular structure. Its solubility can be influenced by several factors, which include:

  • Polarity: 2-nitronon-2-ene contains a nitro functional group that enhances its polarity, allowing it to interact with polar solvents.
  • Temperature: Solubility generally increases with temperature; thus, heating a solution may help dissolve this compound more effectively.
  • Solvent Choice: This compound is better soluble in polar solvents such as water, alcohols, and acetone compared to nonpolar solvents.

To summarize, the solubility characteristics of 2-nitronon-2-ene can be described as notably variable, depending on the conditions under which it is assessed. Considering its usage and interactions in various chemical environments can aid chemists in predicting its behavior effectively. As always, it is essential to conduct solubility tests in specific contexts to better understand its properties.

Interesting facts

Interesting Facts About 2-Nitronon-2-ene

2-Nitronon-2-ene is a fascinating organic compound that intrigues chemists due to its unique structure and potential applications. Here are some noteworthy insights:

  • Unsaturation and Reactivity: The presence of a double bond in 2-nitronon-2-ene makes it an alkene. This unsaturation allows the compound to participate in various chemical reactions, including addition reactions that can create different derivatives with interesting properties.
  • Electrophilic Reactivity: The nitro group (–NO2) attached to the carbon chain enhances the compound's ability to undergo electrophilic aromatic substitution and nucleophilic reactions. As emphasized by many organic chemists, “the more polar a functional group, the more reactive it can become!”
  • Synthetic Utility: 2-Nitronon-2-ene can serve as an important intermediate in the synthesis of various chemical products, including pharmaceuticals and agrochemicals. Its structure makes it a useful building block for designing new compounds with biological activity.
  • Environmental Impact: As with many nitro compounds, it’s essential to consider the environmental implications. The stability of the nitro group can lead to concerns regarding pollutant persistence, making understanding its degradation pathways vital.
  • Research Application: This compound plays a crucial role in research focused on organic synthesis and materials science, helping scientists to develop new methodologies for organic transformations.

Overall, 2-nitronon-2-ene exemplifies the intersection of fundamental chemistry and practical applications. Its unique properties continue to inspire innovations in synthetic strategies and environmental chemistry.

Synonyms
2-nitro-non-2-ene
DTXSID201032307