Skip to main content

2-(4-Chloro-2-nitrophenylazo)malononitrile

ADVERTISEMENT
Identification
Molecular formula
C9H4ClN5O2
CAS number
1994-39-4
IUPAC name
2-(4-chloro-2-nitro-phenyl)azopropanedinitrile
State
State

At room temperature, this compound is typically in a solid crystalline state.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
244.61g/mol
Molar mass
244.6070g/mol
Density
1.6500g/cm3
Appearence

This compound typically appears as a yellow to orange crystalline solid.

Comment on solubility

Solubility of 2-(4-chloro-2-nitro-phenyl)azopropanedinitrile

The solubility of 2-(4-chloro-2-nitro-phenyl)azopropanedinitrile in various solvents can be influenced by its chemical structure and functional groups. This compound comprises both hydrophobic and polar characteristics, which play a significant role in determining its solubility.

General Solubility Characteristics:

  • Polar solvents: Due to the presence of nitro groups (-NO2) and cyano groups (-C≡N), this compound shows some level of solubility in polar solvents such as water and ethanol.
  • Non-polar solvents: It tends to have better solubility in organic non-polar solvents like hexane or dichloromethane, attributable to its aromatic rings which are hydrophobic in nature.
  • Environmental pH: The solubility can also be affected by the pH of the environment, especially considering the presence of acidic or basic conditions that may alter the compound's ionization state.

As a practical guide, one might refer to the rule of thumb: “like dissolves like.” This means compounds with similar polarity are more likely to be soluble in one another. Therefore, the solubility of 2-(4-chloro-2-nitro-phenyl)azopropanedinitrile can be generally described as exhibiting variable solubility based on solvent choice.

In summary, it's essential to experiment with various solvents while considering the compound's specific properties for more accurate solubility information.

Interesting facts

Interesting Facts About 2-(4-Chloro-2-nitro-phenyl)azopropanedinitrile

This intriguing compound, 2-(4-chloro-2-nitro-phenyl)azopropanedinitrile, presents a fascinating mix of chemical properties and applications that capture the attention of chemists. Here are some key highlights:

  • Mechanism of Action: The nitro group in the structure can play a significant role in the biological activity of this compound, often influencing its reactivity and interaction with biological systems.
  • Versatile Applications: Due to its unique structure, this compound can be explored in various fields such as:
    • Agriculture: where it may be developed as a potential agrochemical.
    • Pharmaceuticals: as a lead compound in the synthesis of drugs.
    • Material Science: owing to its potential use in polymer chemistry.
  • Environmental Considerations: The presence of chlorine raises discussions on the environmental impact of its synthesis and application, encouraging research into sustainable alternatives.
  • Synthetic Pathways: The synthesis of this compound highlights the importance of aromatic chemistry and the use of substitution reactions to introduce functional groups.

As quoted by leading researchers in the field, "Understanding the properties of azo compounds can lead to the development of innovative materials that play crucial roles in modern technology." This encapsulates the significance of 2-(4-chloro-2-nitro-phenyl)azopropanedinitrile in chemical research.

In summary, this compound’s structure not only provides intriguing insights into the interactions of nitro and azole groups but also serves as a potential cornerstone for advancements in various scientific domains.

Synonyms
MALONONITRILE, ((4-CHLORO-2-NITROPHENYL)AZO)-
6017-52-3
((4-Chloro-2-nitrophenyl)azo)malonontrile
4-Chlor-2-nitro-phenyl-azo-malonitril [German]
4-Chlor-2-nitro-phenyl-azo-malonitril