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1-Fluoro-4-(2-nitroprop-1-enyl)benzene

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Identification
Molecular formula
C9H8FNO2
CAS number
702-34-9
IUPAC name
1-fluoro-4-(2-nitroprop-1-enyl)benzene
State
State

At room temperature, 1-Fluoro-4-(2-nitroprop-1-enyl)benzene is a liquid.

Melting point (Celsius)
5.00
Melting point (Kelvin)
278.15
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.15
General information
Molecular weight
181.16g/mol
Molar mass
181.1730g/mol
Density
1.1779g/cm3
Appearence

1-Fluoro-4-(2-nitroprop-1-enyl)benzene typically appears as a pale yellow liquid. The liquid form is slightly viscous and possesses a characteristic aromatic odor.

Comment on solubility

Solubility of 1-fluoro-4-(2-nitroprop-1-enyl)benzene

1-fluoro-4-(2-nitroprop-1-enyl)benzene is an organic compound with unique solubility characteristics influenced by its functional groups. Here are some key aspects regarding its solubility:

  • Aromatic Structure: The benzene ring tends to be hydrophobic, generally limiting solubility in polar solvents.
  • Fluoro Group: The presence of the –F atom can enhance solubility in certain polar organic solvents, such as acetone and acetonitrile.
  • Nitro Group: The –NO2 group is polar and contributes to the potential for solubility in water. However, its overall solubility profile may still be restricted due to the bulkiness of the molecule.
  • Compound Interaction: Solubility can be affected by hydrogen bonding and dipole interactions with solvents, making it soluble in mixtures where such interactions can occur.

Overall, while 1-fluoro-4-(2-nitroprop-1-enyl)benzene may exhibit some solubility in a range of solvents, it is expected to be predominantly soluble in non-polar and weakly polar organic solvents, rather than in water.

In summary, understanding the solubility of this compound requires careful consideration of its molecular structure and the nature of the solvents used.

Interesting facts

Interesting Facts About 1-Fluoro-4-(2-nitroprop-1-enyl)benzene

1-Fluoro-4-(2-nitroprop-1-enyl)benzene is a fascinating compound that blends elements of both fluorine chemistry and aromatic compounds. Here are some noteworthy aspects:

  • Functional Groups: The presence of a fluoro group and a nitro group on the aromatic ring significantly influences the reactivity and properties of this compound. Fluorine is known for enhancing electrophilicity, while the nitro group can serve as a strong electron-withdrawing group.
  • Synthetic Utility: Compounds like 1-fluoro-4-(2-nitroprop-1-enyl)benzene are often used in organic synthesis. The unique combination of substituents can lead to interesting pathways for creating more complex molecules.
  • Pharmaceutical Relevance: Many fluorinated compounds, including those featuring nitro groups, have found roles in medicinal chemistry. They can exhibit enhanced biological activity and selectivity, making them important in drug design.
  • Role in Agrochemicals: The reactivity of such compounds often lends itself to applications in agrochemicals, where they may be used as intermediates in the synthesis of pesticides and herbicides.

As a chemist or a student of chemistry, understanding compounds like 1-fluoro-4-(2-nitroprop-1-enyl)benzene not only highlights the versatility of organic molecules but also underscores the significance of functional groups in determining chemical properties.

"Chemistry is the creativity of science." Exploring such compounds fosters a deeper appreciation of the complexities and capabilities within organic chemistry.


Synonyms
775-31-5
1-Fluoro-4-(2-nitro-1-propen-1-yl)benzene
1-fluoro-4-(2-nitroprop-1-en-1-yl)benzene
Maybridge1_007306
VOAXWARMFBBINZ-UHFFFAOYSA-N
DTXSID101271508
AKOS024319151
1-fluoro-4-(2-nitro-1-propenyl)benzene
DB-056225
1-Fluoro-4-[(1E)-2-nitro-1-propenyl]benzene