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2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline

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Identification
Molecular formula
C10H10F3N3O4
CAS number
699-11-2
IUPAC name
2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline
State
State

At room temperature, the compound is in a solid state due to its crystalline form and relatively high melting point of 96.5 °C.

Melting point (Celsius)
96.50
Melting point (Kelvin)
369.65
Boiling point (Celsius)
305.50
Boiling point (Kelvin)
578.65
General information
Molecular weight
292.19g/mol
Molar mass
292.1840g/mol
Density
1.5600g/cm3
Appearence

2,6-Dinitro-N-propyl-4-(trifluoromethyl)aniline is a bright yellow crystalline solid. The compound is known for its vivid color which makes it distinct in appearance, and it is typically crystalline in form.

Comment on solubility

Solubility of 2,6-Dinitro-N-propyl-4-(trifluoromethyl)aniline

The solubility of 2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline in various solvents presents some intriguing characteristics. This compound is known to be:

  • Moderately soluble in organic solvents: Solvents such as acetone, ethanol, and dichloromethane exhibit good affinity for this compound due to its non-polar trifluoromethyl group.
  • Poorly soluble in water: The presence of nitro groups tends to diminish the overall solubility in polar solvents like water, making it less favorable for dissolution.
  • Influenced by temperature: As with many organic compounds, increasing the temperature can enhance solubility, particularly in organic solvents, allowing for greater molecular interaction.

In practice, when attempting to dissolve 2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline, it is advisable to consider:

  1. Choice of solvent: Opting for a non-polar organic solvent aids in achieving better solubility.
  2. Concentration: Dilute solutions might exhibit different solubility characteristics compared to concentrated forms.
  3. Experimental conditions: Factors such as agitation and temperature can significantly impact the efficiency of dissolution.

In conclusion, understanding the solubility behavior of 2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline is essential for its application in various chemical processes and formulations. A careful approach to selecting the appropriate solvent and conditions is crucial for optimizing its use in research and industry.

Interesting facts

Interesting Facts About 2,6-Dinitro-N-propyl-4-(trifluoromethyl)aniline

2,6-Dinitro-N-propyl-4-(trifluoromethyl)aniline, often referred to in the context of its functional importance in the field of chemistry, showcases a remarkable array of properties and applications. This compound is a derivative of aniline, which is a significant building block in organic chemistry. Here are some engaging points about this compound:

  • Structure and Substitution: The compound features two nitro groups and a trifluoromethyl group attached to its aromatic ring. This unique substitution pattern contributes to interesting electronic and steric effects, influencing its reactivity and interaction with other molecules.
  • Applications: Compounds like 2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline have potential applications in the development of herbicides and pesticides, showcasing their importance in agriculture.
  • Impact on Chemical Properties: The presence of electronegative groups such as nitro and trifluoromethyl can enhance lipophilicity and alter the environmental fate of the compound, making it a subject of study for its behavior in biological systems.
  • Research Tool: This compound may serve as a valuable research tool in the synthesis of other complex molecules. It can act as a precursor in creating a variety of functionalized products, which are essential in materials science and medicinal chemistry.
  • Regulatory Considerations: Due to its chemical nature, compounds containing nitro groups often attract regulatory scrutiny, making it essential to study their toxicity and environmental impact.

As researchers delve deeper into the properties and utilities of 2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline, they uncover not only its chemical significance but also its role in advancing fields like pharmaceutical development and agrochemical innovation.

In the words of a renowned chemist, "Understanding the intricacies of a compound's structure allows us to unlock its potential and boundaries in applications." Thus, the exploration of such compounds is not only about their current uses but also their futuristic implications in science.

Synonyms
2077-99-8
Benzenamine, 2,6-dinitro-N-propyl-4-(trifluoromethyl)-
2,6-Dinitro-N-propyl-4-(trifluoromethyl)benzenamine
DTXSID90174840
DTXCID9097331
2,6-dinitro-N-propyl-4-(trifluoromethyl)aniline
SCHEMBL11574765
QXXIZJPWGJDHKR-UHFFFAOYSA-N
AKOS001033708
(Dinitro-trifluoromethyl-phenyl)-propyl-amine
NS00067843
SR-01000025615
SR-01000025615-1
2,6-dinitro-N-propyl-4-(trifluoro-methyl)benzenamine
Z55324415