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2-Nitroprop-1-enylbenzene

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Identification
Molecular formula
C9H9NO2
CAS number
573-54-4
IUPAC name
2-nitroprop-1-enylbenzene
State
State

At room temperature, 2-nitroprop-1-enylbenzene is generally a liquid. It remains stable in this phase under standard conditions of temperature and pressure.

Melting point (Celsius)
-27.00
Melting point (Kelvin)
246.15
Boiling point (Celsius)
269.00
Boiling point (Kelvin)
542.15
General information
Molecular weight
163.17g/mol
Molar mass
163.1840g/mol
Density
1.1074g/cm3
Appearence

2-Nitroprop-1-enylbenzene is a yellow liquid. It has a characteristic aromatic odor and may appear oily. Its appearance can vary slightly depending on its purity and the presence of other compounds, but it generally maintains a consistent yellow color in its pure form.

Comment on solubility

Solubility of 2-Nitroprop-1-enylbenzene

2-Nitroprop-1-enylbenzene, with its unique structure, presents several intriguing characteristics in terms of solubility. Here are some key points to consider:

  • Polarity: The presence of the nitro group (-NO2) contributes to the overall polarity of the molecule, which can enhance its solubility in polar solvents.
  • Hydrophobic Interactions: The benzene ring, as a hydrophobic component, may lead to reduced solubility in water.
  • Solvent Compatibility: This compound tends to dissolve better in organic solvents such as ethanol and acetone, which are less polar than water.

Overall, the solubility of 2-nitroprop-1-enylbenzene is markedly influenced by its molecular structure. As a general rule, like dissolves like—thus, it is more effectively soluble in organic solvents compared to aqueous solutions. Understanding the solubility characteristics of this compound is essential for its applications in various chemical processes.

Interesting facts

Interesting Facts about 2-Nitroprop-1-enylbenzene

2-Nitroprop-1-enylbenzene is an intriguing compound that falls into the category of nitro-substituted aromatic hydrocarbons. Here are some noteworthy aspects of this compound:

  • Structure and Reactivity: The compound possesses a unique structure that features both a nitro group and a prop-1-enyl chain attached to a benzene ring. This combination contributes to its reactivity and potential applications in organic synthesis.
  • Multi-functional Applications: Due to its functional groups, 2-nitroprop-1-enylbenzene can serve as a valuable intermediate in the synthesis of various chemical compounds, particularly in pharmaceuticals and agrochemicals.
  • Electronic Effects: The presence of the nitro group has a significant influence on the electron density of the benzene ring, which can alter the compound's chemical behavior and reactivity. Nitro groups are known to be strong electron-withdrawing groups.
  • Potential Biological Activity: Compounds similar to 2-nitroprop-1-enylbenzene have been studied for their biological properties, including antibacterial and antitumor activities, making them of interest in medicinal chemistry.
  • Environmental Considerations: Like many nitro compounds, this compound may pose environmental challenges due to potential toxicity and persistence in the environment. Scientists are continuously researching methods to mitigate such effects.

In summary, 2-nitroprop-1-enylbenzene exemplifies the complexity and utility of nitro-substituted aromatic compounds in chemical research and applications. Its interesting properties contribute to ongoing studies in both synthetic chemistry and environmental science.

Synonyms
2-NITRO-1-PHENYLPROPENE
2-nitro-3-phenyl-2-propene
(2-nitro-propenyl)-benzene
Maybridge1_007263
?-METHYL B-NITROSTYRENE
WGSVFWFSJDAYBM-UHFFFAOYSA-N
(Z)-1-(2-nitroprop-1-enyl)benzene
AKOS017269182
SY076962
DB-006200
A9304
NS00067944