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4-nitrohept-3-ene

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Identification
Molecular formula
C7H13NO2
CAS number
3371-82-4
IUPAC name
4-nitrohept-3-ene
State
State

At room temperature, 4-nitrohept-3-ene is in a liquid state.

Melting point (Celsius)
-36.00
Melting point (Kelvin)
237.15
Boiling point (Celsius)
218.00
Boiling point (Kelvin)
491.15
General information
Molecular weight
157.19g/mol
Molar mass
157.1870g/mol
Density
1.0552g/cm3
Appearence

4-Nitrohept-3-ene is typically a liquid at room temperature. Its appearance can be characterized by having a clear to yellowish color. As with many nitro compounds, it may have a slight odor that is typical of nitro compounds.

Comment on solubility

Solubility of 4-Nitrohept-3-ene

4-Nitrohept-3-ene, with the chemical formula C7H11NO2, is a compound that presents interesting features regarding its solubility. The solubility of such organic compounds can often depend on several factors:

  • Polarity: 4-Nitrohept-3-ene has both a long hydrophobic carbon chain and a polar nitro group. This dual nature can lead to solubility in both polar and non-polar solvents, though it may be more soluble in polar organic solvents like ethanol or acetone.
  • Hydrogen Bonding: The presence of the nitro group may allow for some hydrogen bonding with solvents, enhancing solubility in polar conditions.
  • Temperature: Like many organic molecules, the solubility can increase with temperature, potentially allowing for better dissolution in various solvents at higher conditions.

In summary, while specific experimental solubility data for 4-nitrohept-3-ene may be limited, its structural features suggest that it can significantly interact with polar solvents. Thus, it can be categorized as having moderate solubility characteristics, suitable for a range of applications in organic chemistry.

Interesting facts

Interesting Facts About 4-Nitrohept-3-ene

4-Nitrohept-3-ene is a fascinating organic compound that showcases the diversity and complexity of chemical structures within the field of organic chemistry. Here are some intriguing aspects of this compound:

  • Functional Groups: The presence of a nitro group (–NO2) gives this compound unique chemical properties, including its potential reactivity and role in various chemical reactions.
  • Applications in Research: Compounds like 4-nitrohept-3-ene are often studied for their utility in synthesizing more complex molecules, especially in pharmaceuticals and agrochemicals.
  • Stereochemistry: As an alkene, 4-nitrohept-3-ene possesses a double bond which can exhibit geometric isomerism. This aspect can lead to different physical and chemical properties based on the configuration of substituents around the double bond.
  • Environmental Considerations: Nitro compounds can sometimes raise concerns regarding their environmental impact and bioaccumulation, prompting research into safer alternatives and degradation pathways.
  • Electronic Effects: The presence of a nitro group can significantly influence the electron density across the compound, affecting its reactivity and interaction with other chemical species.

In conclusion, 4-nitrohept-3-ene is a prime example of how subtle changes in molecular structure can lead to vast differences in properties and applications. Its study not only broadens our understanding of organic compounds but also stimulates advances in various applied sciences.

Synonyms
4-nitro-hept-3-ene