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Dinitrobutylphenyl ether

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Identification
Molecular formula
C19H26N2O6
CAS number
136-78-7
IUPAC name
[2,6-dinitro-4-(1,1,4-trimethylpentyl)phenyl] but-2-enoate
State
State

The compound is in its solid state at room temperature.

Melting point (Celsius)
88.00
Melting point (Kelvin)
361.15
Boiling point (Celsius)
384.00
Boiling point (Kelvin)
657.15
General information
Molecular weight
367.40g/mol
Molar mass
367.4040g/mol
Density
1.2800g/cm3
Appearence

The compound typically appears as a yellow crystalline solid. The presence of nitro groups often imparts a characteristic color and solid state.

Comment on solubility

Solubility of [2,6-dinitro-4-(1,1,4-trimethylpentyl)phenyl] but-2-enoate

The solubility of [2,6-dinitro-4-(1,1,4-trimethylpentyl)phenyl] but-2-enoate can be characterized by several key points:

  • General Behavior: This compound is largely hydrophobic due to its extensive organic structure, suggesting low solubility in water.
  • Solvent Compatibility: It is expected to be more soluble in non-polar organic solvents such as hexane, toluene, or chloroform.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, particularly in organic solvents, enabling better interactions with solvent molecules.
  • Influence of Functional Groups: The presence of nitro groups can also affect solubility by introducing polar characteristics, albeit limited.

In summary, while [2,6-dinitro-4-(1,1,4-trimethylpentyl)phenyl] but-2-enoate may exhibit some degree of solubility in specific polar environments, its primary solubility traits lie within the realm of organic, non-polar solvents. Understanding these solubility characteristics is essential for applications in chemical formulations and synthesis.

Interesting facts

Interesting Facts About [2,6-dinitro-4-(1,1,4-trimethylpentyl)phenyl] but-2-enoate

This compound, bearing a complex structure, is a member of the nitroaromatic family and possesses unique characteristics that make it a fascinating subject of study in chemistry. Here are some key points worth noting:

  • Applications: It finds use in various fields, especially in organic synthesis and as an intermediate in the production of other chemical compounds.
  • Reactivity: The presence of nitro groups can significantly influence the reactivity of this compound, making it valuable in electrophilic substitution reactions.
  • Environmental Concerns: Nitro compounds are of concern due to their potential toxicity and environmental impact. Studying their degradation pathways can provide insight into mitigating pollution.
  • Synthesis: The synthesis of this compound can involve multiple steps, including nitration and alkylation processes, which offer a practical challenge for chemists.

As we dive deeper into its structure, we can appreciate the *intricate balance between its stability and reactivity* provided by its substituents. The bulky 1,1,4-trimethylpentyl group not only adds steric hindrance but also influences the compound's overall characteristics. This compound serves as a remarkable example of how variations in molecular structure can lead to diverse chemical behavior, offering rich avenues for research and application.

In summary, studying [2,6-dinitro-4-(1,1,4-trimethylpentyl)phenyl] but-2-enoate can foster a greater understanding of both synthetic and applied chemistry, highlighting the intricate dance of molecular interactions.