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4-Chloro-N-(4-methoxybenzylidene)aniline

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Identification
Molecular formula
C14H12ClNO
CAS number
2629-22-9
IUPAC name
4-chloro-N-[(4-methoxyphenyl)methyleneamino]aniline
State
State

This compound is typically a solid at room temperature. It maintains its solid-state under normal atmospheric conditions and does not liquefy or vaporize unless subjected to higher temperatures close to its melting point or boiling point respectively.

Melting point (Celsius)
104.00
Melting point (Kelvin)
377.15
Boiling point (Celsius)
406.40
Boiling point (Kelvin)
679.55
General information
Molecular weight
247.71g/mol
Molar mass
247.7050g/mol
Density
1.2900g/cm3
Appearence

4-Chloro-N-(4-methoxybenzylidene)aniline typically appears as a solid crystalline compound. The crystals can vary but are often observed in shades ranging from pale yellow to off-white. Its crystalline nature is noticeable under magnification, where the distinct, structured geometric shapes can be seen.

Comment on solubility

Solubility of 4-chloro-N-[(4-methoxyphenyl)methyleneamino]aniline

The solubility of 4-chloro-N-[(4-methoxyphenyl)methyleneamino]aniline in various solvents can be influenced by its unique structural features. This compound, with multiple functional groups, exhibits intriguing solubility behavior due to the balance between hydrophilic and hydrophobic attributes.

Factors Affecting Solubility:

  • Polarity: The presence of the chloro and methoxy groups can affect the overall polarity, leading to varied solubility in polar and nonpolar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds may enhance solubility in polar solvents like water, while also impacting solubility in organic solvents.
  • Molecular Size: The size of the compound can create steric hindrance, potentially limiting solubility in certain solvents.

When discussing solubility, it is essential to refer to common solvents:

  • Water: Solubility can be moderate; the methoxy group may facilitate some solubility, while the chloro group can introduce hydrophobic characteristics.
  • Organic Solvents: Likely to demonstrate better solubility in solvents such as ethanol or dimethyl sulfoxide (DMSO) due to their ability to solvate the compound effectively.

In summary, while specific solubility data may vary and require empirical testing, understanding the interplay of structural elements is crucial in predicting the behavior of 4-chloro-N-[(4-methoxyphenyl)methyleneamino]aniline in different solvent environments.

Interesting facts

Interesting Facts about 4-chloro-N-[(4-methoxyphenyl)methyleneamino]aniline

The compound 4-chloro-N-[(4-methoxyphenyl)methyleneamino]aniline is notable for its intriguing chemical structure and potential applications in various fields. Understanding its characteristics can unveil a world of possibilities in both research and industry. Here are some fascinating points about this compound:

  • Versatile Intermediate: This compound is often explored as an intermediate in the synthesis of various pharmaceutical agents, owing to its unique configuration of functional groups.
  • Bioactivity: Researchers have indicated that compounds with similar structures may exhibit significant biological activities, including antimicrobial and anticancer properties. This could open doors for the development of new therapeutic agents.
  • Electronics and Polymers: The electronically rich aromatic rings in this molecule suggest potential applications in organic electronics and related polymeric materials, making it of interest for material scientists.
  • Research Relevance: The chlorine and methoxy substituents may provide unique reactivity patterns in chemical reactions, which chemists study to create novel compounds and materials.
  • Analytical Chemistry: The structure of this compound allows for its identification and quantification using various analytical techniques, making it a useful model compound in studies of analytical chemistry.

In summary, 4-chloro-N-[(4-methoxyphenyl)methyleneamino]aniline serves as more than just a chemical entity—it's a potential gateway for innovative discoveries across multiple scientific disciplines. The exploratory avenues for research are abundant, enhancing our understanding of both organic synthesis and medicinal chemistry.

Synonyms
AKOS034405199