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N-(2-chloroprop-2-enylideneamino)-2,4-dinitroaniline

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Identification
Molecular formula
C9H9ClN4O4
CAS number
215456-17-4
IUPAC name
N-(2-chloroprop-2-enylideneamino)-2,4-dinitro-aniline
State
State

At room temperature, N-(2-chloroprop-2-enylideneamino)-2,4-dinitroaniline exists in a solid state. It is typically handled in powdered or crystalline form, demonstrating stability under normal conditions.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
271.64g/mol
Molar mass
271.6350g/mol
Density
1.5412g/cm3
Appearence

N-(2-chloroprop-2-enylideneamino)-2,4-dinitroaniline typically appears as a yellow to orange crystalline solid. Its vivid coloration is owed to the presence of nitro groups, which often impart bright colors to aromatic compounds.

Comment on solubility

Solubility Insights for N-(2-chloroprop-2-enylideneamino)-2,4-dinitro-aniline

N-(2-chloroprop-2-enylideneamino)-2,4-dinitro-aniline is a complex organic compound, which can pose unique challenges when it comes to solubility. Understanding its solubility behavior is crucial in various applications, including synthesis and formulation. Here are some key points to consider:

  • Polarity: The presence of numerous functional groups, such as amino and nitro groups, suggests that this compound may exhibit polar characteristics. Generally, polar compounds dissolve well in polar solvents.
  • Hydrogen Bonding: The amino group can form hydrogen bonds, potentially increasing solubility in polar solvents like water and alcohols.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF), which can solvate both polar and non-polar regions of the molecule.
  • Temperature Dependence: Solubility may vary with temperature; often, heating a solvent can improve the solubility of organic compounds.

In summary, the solubility of N-(2-chloroprop-2-enylideneamino)-2,4-dinitro-aniline is influenced by its molecular structure, polarity, and the choice of solvent. A practical approach to determining its solubility would be to assess it in a range of solvents under controlled conditions, taking into account the factors mentioned above.

Interesting facts

Exploring N-(2-Chloroprop-2-enylideneamino)-2,4-dinitro-aniline

N-(2-Chloroprop-2-enylideneamino)-2,4-dinitro-aniline is a unique compound with intriguing properties and applications. Here are some fascinating aspects of this compound:

  • Functional Versatility: This compound contains an amino group and multiple nitro groups, making it a potential candidate for a variety of chemical reactions. Such functionalities allow for its use in synthesizing other complex organic molecules.

  • Potential Role in Pharmaceuticals: Compounds featuring dinitroaniline structures are frequently studied for their biological activities. Researchers are investigating their potential as therapeutic agents, particularly in the field of cancer research.

  • Environmental Considerations: Given the presence of nitro groups, there may be concerns regarding the environmental impact and degradation of this compound. Understanding its stability and breakdown products is crucial for assessing its ecological footprint.

  • Applications in Dyes: Chemical compounds with similar structures have been employed in the textile industry as dye intermediates. They play a significant role in producing vibrant colors, making them valuable for applications in fashion and design.

  • Reactivity and Stability: The presence of chlorine and nitro groups can influence the reactivity patterns of this molecule, leading to a spectrum of asymmetrical reactions that are of great interest in organic chemistry. They also affect the compound's stability and interaction with other chemical agents.

The study of N-(2-chloroprop-2-enylideneamino)-2,4-dinitro-aniline not only highlights its chemical versatility but also raises questions about safety, efficacy, and environmental impact. As scientists delve deeper into this compound, they continue to unearth its potential and pave the way for innovative applications in chemistry and beyond.

Synonyms
2-chloroacrolein 2,4-dinitrophenylhydrazone