Skip to main content

4-Nitrophenyl cyclohexanecarboxylate

ADVERTISEMENT
Identification
Molecular formula
C13H15NO4
CAS number
7403-75-6
IUPAC name
(4-nitrophenyl) cyclohexanecarboxylate
State
State

The compound is typically a solid at room temperature. It forms yellow crystalline structures.

Melting point (Celsius)
83.00
Melting point (Kelvin)
356.15
Boiling point (Celsius)
398.00
Boiling point (Kelvin)
671.15
General information
Molecular weight
247.27g/mol
Molar mass
247.2720g/mol
Density
1.2800g/cm3
Appearence

4-Nitrophenyl cyclohexanecarboxylate appears as a yellow crystalline solid. The compound's color is attributed to the nitro group attached to the phenyl ring.

Comment on solubility

Solubility of (4-nitrophenyl) cyclohexanecarboxylate

The solubility of (4-nitrophenyl) cyclohexanecarboxylate can be influenced by various factors, making it an interesting compound to study. Here are some key points regarding its solubility:

  • Polarity: The presence of a nitro group (-NO2) can increase the polarity of the molecule, which may enhance solubility in polar solvents.
  • Hydrophobicity: The cyclohexanecarboxylate moiety tends to exhibit hydrophobic characteristics, potentially limiting solubility in polar solvents.
  • Solvent Interaction: This compound may show varying solubility in protic versus aprotic solvents. Thus, studying its behavior in different solvents can yield valuable insights.
  • Temperature Dependency: Like many organic compounds, solubility can vary with temperature, often increasing at elevated temperatures.

In summary, the solubility of (4-nitrophenyl) cyclohexanecarboxylate is a balance of its polar and nonpolar characteristics, dependent on the solvent used. As with many organic compounds, understanding its solubility profile can shed light on its behavior in different environments, which is crucial for applications in pharmaceuticals and materials science.

Interesting facts

Interesting Facts about (4-Nitrophenyl) Cyclohexanecarboxylate

(4-Nitrophenyl) cyclohexanecarboxylate is a fascinating compound characterized by its unique structure and a variety of applications in the field of chemistry. Here are some engaging insights into this compound:

  • Structural Features: This compound consists of a cyclohexane ring connected to a carboxylate group and a nitrophenyl group. The presence of both the nitro and carboxylate functional groups significantly influences its chemical reactivity and physical properties.
  • Reactivity: The nitro group attached to the phenyl ring isn’t just for decoration—but it enhances the electrophilicity of the aromatic system, making (4-nitrophenyl) cyclohexanecarboxylate a valuable intermediate in organic synthesis reactions.
  • Applications: This compound is often employed in the synthesis of more complex organic molecules, particularly in pharmaceuticals and agrochemicals. The versatility of the functional groups enables its use in various synthetic pathways.
  • Research Significance: Scientists have shown interest in compounds like (4-nitrophenyl) cyclohexanecarboxylate as they can serve as model compounds for studying reaction mechanisms involving aromatic substitutions, as well as for investigations into molecular interactions.
  • Environmental Considerations: However, the usage of nitro groups often raises concerns about toxicity and environmental impact, prompting ongoing research into safer and greener alternatives while still maintaining similar reactivity.

In summary, (4-nitrophenyl) cyclohexanecarboxylate is not just another chemical compound; it embodies the intricate intersection of structure, reactivity, and application, making it a notable subject of study in both academic and industrial chemistry.

Synonyms
P-NITROPHENYL CYCLOHEXANECARBOXYLATE
13551-17-2
Cyclohexanecarboxylic acid, 4-nitrophenyl ester
4-nitrophenyl cyclohexanoate
SCHEMBL9836028
SCHEMBL11602621
DTXSID50159431
UCQFTYKBLBJWIO-UHFFFAOYSA-N
Cyclohexanecarboxylic acid 4-nitro-phenyl ester