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2-phenylazopropanedinitrile

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Identification
Molecular formula
C11H6N4
CAS number
135-61-5
IUPAC name
2-phenylazopropanedinitrile
State
State

At room temperature, 2-phenylazopropanedinitrile is typically found as a solid. It is stable under standard temperatures and pressures and generally requires specific solvents or conditions for dissolution.

Melting point (Celsius)
139.00
Melting point (Kelvin)
412.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
181.18g/mol
Molar mass
181.1750g/mol
Density
1.1500g/cm3
Appearence

2-phenylazopropanedinitrile appears as a solid compound ranging in color from orange to red. The vivid coloration is characteristic of many azo compounds, which are known for their intense hues due to the presence of the azo group (-N=N-) often conjugated with aromatic systems. The appearance of this compound can vary slightly depending on its crystalline form and level of purity.

Comment on solubility

Solubility of 2-phenylazopropanedinitrile

2-phenylazopropanedinitrile, with the chemical formula C12H10N4, exhibits interesting solubility characteristics that make it an intriguing compound for various applications.

Solubility in Various Solvents

This compound is primarily soluble in organic solvents, which can be attributed to its non-polar characteristics. The following points highlight its solubility behavior:

  • Non-polar Solvents: It shows good solubility in non-polar solvents such as hexane and ether.
  • Polar Solvents: Its solubility in polar solvents like water is limited, highlighting its hydrophobic nature.
  • Mixed Solvents: In mixed solvent systems, the solubility can vary significantly depending on the proportion of the solvents used.

Factors Influencing Solubility

The solubility of 2-phenylazopropanedinitrile can be influenced by several factors:

  • Temperature: Generally, increased temperatures lead to enhanced solubility in solvents.
  • pH Levels: In some cases, changes in pH can affect the ionization of the compound, thus influencing its solubility.
  • Presence of Other Chemicals: Certain solutes can either aid or hinder solubility through competitive interactions.

Conclusion

In summary, 2-phenylazopropanedinitrile showcases a distinct solubility profile that is heavily dependent on the solvent system used. Its modest solubility in polar environments alongside better solubility in organic solvents underscores its potential applications in chemical synthesis and material science. Understanding its solubility can aid researchers in effectively utilizing this compound in various studies and applications.

Interesting facts

Interesting Facts about 2-Phenylazopropanedinitrile

2-Phenylazopropanedinitrile is a fascinating compound that has caught the attention of chemists and researchers alike due to its unique structure and properties. Here are some interesting aspects of this compound:

  • Structure: This compound features an azo group, which consists of a nitrogen-nitrogen double bond. The presence of the phenyl group contributes to its distinct properties.
  • Applications: 2-Phenylazopropanedinitrile is commonly used in the synthesis of various organic compounds. Its reactivity makes it a valuable intermediate in organic chemistry.
  • Chemical Behavior: This compound exhibits interesting reactivity patterns due to the presence of the dinitrile functional groups. These characteristics provide insights into mechanisms of substitution reactions.
  • Synthetic Pathways: Chemists often explore diverse synthetic pathways to produce 2-Phenylazopropanedinitrile, enhancing their understanding of organic synthesis techniques.
  • Color Chemistry: Azo compounds are known for their vivid color properties. While 2-Phenylazopropanedinitrile may not be directly used as a dye itself, studying its derivates can deepen our knowledge of color chemistry.

Overall, 2-Phenylazopropanedinitrile stands as a compound of considerable interest in the realm of organic chemistry, presenting opportunities for exploration and innovation in both academic and industrial settings.

As noted by one chemist, “The real beauty of compounds like 2-Phenylazopropanedinitrile lies not just in their structure, but in the myriad of ways we can manipulate them to create new materials.”

Synonyms
6017-21-6
2-(2-Phenyldiazenyl)propanedinitrile
DTXSID101289496
DTXCID401280112
809-856-7
Benzeneazomalononitrile
(Phenylazo)malononitrile
2-(Phenylazo)malononitrile
2-phenyldiazenylpropanedinitrile
(E)-2-(phenyldiazenyl)Malononitrile
Propanedinitrile, (phenylazo)-
2-(phenyldiazenyl)malononitrile
phenylazomalononitrile
MALONONITRILE, (PHENYLAZO)-
2-[(E)-2-phenyldiazen-1-yl]propanedinitrile
1350653-31-4
NSC-263832
NSC 263832
Phenyl-azo-malonitril
Phenyl-azo-malonitril [German]
F 2201
BRN 0957332
MFCD00524838
Riociguat intermediate
Propanedinitrile, 2-(2-phenyldiazenyl)-
2-Phenylazo-malononitrile
[Phenyldiazenyl]malononitrile
Malononitrile, 2-phenylazo-
alpha-(phenylazo)malononitrile
SCHEMBL248649
KLMBASWITNCMTF-UHFFFAOYSA-N
QF95S73B62
BCP11327
CS-M2184
NSC263832
AKOS006241424
AKOS028108402
GS-6863
SB17525
AC-29285
2-[(1E)-2-Phenyldiazenyl]propanedinitrile
2-[(1E)-2-phenyldiazen-1-yl]propanedinitrile
D77447
F11884
Propanedinitrile, 2-[(1E)-2-phenyldiazenyl]-
2-[(1E)-2-PHENYLDIAZENYL]-PROPANEDINITRILE