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N-(allylideneamino)aniline

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Identification
Molecular formula
C9H11N
CAS number
38442-30-7
IUPAC name
N-(allylideneamino)aniline
State
State

At room temperature, N-(allylideneamino)aniline is present in a liquid state. It is typically stored in tightly sealed containers to prevent exposure to air and humidity, which could lead to changes in its state and chemical properties.

Melting point (Celsius)
-19.00
Melting point (Kelvin)
254.15
Boiling point (Celsius)
269.40
Boiling point (Kelvin)
542.55
General information
Molecular weight
147.20g/mol
Molar mass
147.1970g/mol
Density
0.9930g/cm3
Appearence

N-(allylideneamino)aniline is a pale yellow or colorless oily liquid. It may darken upon exposure to air and light, indicating potential oxidation or polymerization reactions affecting its appearance.

Comment on solubility

Solubility of N-(allylideneamino)aniline

N-(allylideneamino)aniline, a compound formed from the interaction of an allyl group with an aniline structure, exhibits certain solubility characteristics that are influenced by its molecular structure and functional groups. When considering solubility, it is essential to note the following points:

  • Polarity: The presence of the amino group (-NH2) contributes to the overall polarity of the compound, which enhances its solubility in polar solvents, particularly water.
  • Hydrophobic Regions: The allylidene group introduces a hydrophobic character, which can limit solubility in highly polar solvents.
  • Solvent Selection: N-(allylideneamino)aniline may exhibit improved solubility in organic solvents like ethanol, methanol, and possibly acetone, where its hydrophobic character is less of a hindrance.
  • Temperature Influence: Solubility may increase with temperature, a common trend with many organic compounds, particularly when transitioning to more complex solvent systems.

In summary, while N-(allylideneamino)aniline can be soluble in both polar and some non-polar solvents, the balance between its hydrophilic and hydrophobic characteristics plays a crucial role in determining its solubility behavior. In practical applications, thorough solvent testing is recommended to ascertain the most effective conditions for dissolution.

Interesting facts

Interesting Facts about N-(Allylideneamino)aniline

N-(Allylideneamino)aniline, a fascinating organic compound, belongs to the class of aromatic amines. Its unique structure lends itself to various applications and interesting properties, making it a noteworthy subject of study in chemistry.

Key Characteristics

  • Reactivity: The presence of both an allyl group and an amino group in its structure provides diverse reactivity options, allowing it to participate in multiple chemical reactions.
  • Versatile Applications: This compound has potential applications in pharmaceuticals, dyes, and other organic synthesis processes.
  • Synthetic Pathways: Researchers often explore various synthetic routes, making it a compound of interest for those studying synthetic organic chemistry.

Chemical Significance

One of the most intriguing aspects of N-(allylideneamino)aniline is its ability to form derivatives. This characteristic is essential for:

  • Developing novel pharmaceutical agents with enhanced biological activity.
  • Creating functionalized materials that can be used in advanced technological applications.

Research Insights

Studies involving N-(allylideneamino)aniline often emphasize its potential in:

  • Interaction with various chemical environments and its role in catalysis.
  • Investigating its properties to design new compounds with desired characteristics.

In summary, N-(allylideneamino)aniline is not just a molecule; it is a gateway to exploring new realms of synthetic chemistry and materials science. As chemists continue to delve into its properties and reactions, one can only imagine the breakthroughs this compound might inspire in the future!

Synonyms
Acrolein-Phenylhydrazon
5834-97-9
Propenal phenylhydrazone
NCIOpen2_000443
SCHEMBL1876865
DTXSID101031932
DB-266659