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2-[(3-Chlorophenyl)hydrazonomethyl]malononitrile

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Identification
Molecular formula
C10H6ClN3
CAS number
71063-91-3
IUPAC name
2-[(3-chlorophenyl)azomethyl]propanedinitrile
State
State

The compound is typically solid at room temperature.

Melting point (Celsius)
67.50
Melting point (Kelvin)
340.65
Boiling point (Celsius)
319.70
Boiling point (Kelvin)
592.85
General information
Molecular weight
187.61g/mol
Molar mass
187.6130g/mol
Density
1.2605g/cm3
Appearence

2-[(3-Chlorophenyl)azomethyl]propanedinitrile appears as a crystalline solid. It is a compound often used in chemical research and synthesis.

Comment on solubility

Solubility of 2-[(3-chlorophenyl)azomethyl]propanedinitrile

When assessing the solubility of 2-[(3-chlorophenyl)azomethyl]propanedinitrile, it is essential to consider a few key factors:

  • Polarity: The compound contains polar nitrile groups (–C≡N), which can enhance its solubility in polar solvents.
  • Hydrophobic Interactions: The presence of a 3-chlorophenyl moiety may introduce some hydrophobic characteristics, making it less soluble in water but potentially soluble in organic solvents.
  • Concentration Effects: As with many organic compounds, the solubility can vary significantly with concentration and temperature. Higher temperatures generally increase solubility in liquids.

In summary, while 2-[(3-chlorophenyl)azomethyl]propanedinitrile is likely to have limited solubility in water due to its hydrophobic components, it may demonstrate reasonable solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), or acetone. Understanding these solubility characteristics is crucial for applications in both laboratory and industrial settings.

Interesting facts

Interesting Facts about 2-[(3-Chlorophenyl)azomethyl]propanedinitrile

2-[(3-Chlorophenyl)azomethyl]propanedinitrile is a fascinating compound primarily recognized for its roles in both industrial applications and research. Here are some intriguing insights:

  • Chemical Structure: The compound features a unique structure where a chlorophenyl group is bonded to an azomethyl chain, making it a valuable derivative in organic synthesis.
  • Biological Activity: Compounds containing azomethyl groups often exhibit notable biological activities. Researchers are continually investigating their potential as antimicrobial and anticancer agents.
  • Versatile Reactions: Due to the presence of multiple nitrile groups, this compound participates in a variety of reactions, including nucleophilic addition and cyclization, which are crucial in synthetic organic chemistry.
  • Application in Material Science: It's explored for its applications in material science, particularly in developing functional materials that can be used in electronics and photonics.
  • Importance in Research: It serves as an interesting intermediate for synthesizing more complex organic molecules, impacting various fields such as pharmaceuticals and agrochemicals.
  • Prototypical Example: This compound is an excellent prototype for understanding the reactivity of substituted nitriles, which are pivotal in the formation of co-crystals and coordination compounds.

Overall, 2-[(3-Chlorophenyl)azomethyl]propanedinitrile is a notable compound in the world of organic chemistry, reflecting the intricate connections between structure, reactivity, and application. As we continue to explore its properties, the potential for new discoveries remains vast!

Synonyms
((m-Chlorophenyl)azo)methylmalononitrile
3655-93-4
F 2284
3-Chlor-phenyl-azo-methyl-malonitril [German]
MALONONITRILE, ((m-CHLOROPHENYL)AZO)METHYL-
3-Chlor-phenyl-azo-methyl-malonitril