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3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline

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Identification
Molecular formula
C14H12BrN2O
CAS number
NULL
IUPAC name
3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline
State
State

At room temperature, 3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline is typically a solid.

Melting point (Celsius)
164.00
Melting point (Kelvin)
437.15
Boiling point (Celsius)
390.20
Boiling point (Kelvin)
663.35
General information
Molecular weight
292.16g/mol
Molar mass
292.1320g/mol
Density
1.4700g/cm3
Appearence

This compound appears as a crystalline solid that may vary in color from off-white to light brown, depending on the purity and method of synthesis. It may exhibit a mild aromatic odor.

Comment on solubility

Solubility of 3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline

The solubility of 3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline in various solvents can provide significant insights into its chemical behavior. Here are some key points to consider:

  • Polar solvents: This compound's solubility in polar solvents like water may be limited due to its organic structure, which includes non-polar aromatic rings that hinder interaction with polar molecules.
  • Non-polar solvents: It is likely to exhibit better solubility in non-polar organic solvents such as toluene or ethyl acetate. The hydrophobic nature of the aromatic rings favors interactions with similar solvents.
  • Solvent interactions: The presence of the bromo group and methoxy group may have varying effects on the overall solubility, influencing hydrogen bonding and dipole-dipole interactions.
  • Temperature effects: Solubility can increase with temperature, as higher energy levels may help overcome lattice energy and enhance dissolution.

An important takeaway is that solubility is not a static property; it often depends on the solvent matrix, temperature, and chemical structure of the compound itself. Understanding these aspects can aid in practical applications and further research into the compound's behavior in different environments.

Interesting facts

Interesting Facts about 3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline

3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline is a fascinating compound that showcases the intricate world of organic chemistry. This compound belongs to the class of anilines, which are renowned for their diverse applications in various fields.

Applications

  • Dyes and Pigments: Anilines are key intermediates in the manufacture of dyes and pigments. The unique structure of this particular compound may contribute to vibrant color properties.
  • Pharmaceuticals: Some derivatives of anilines exhibit significant biological activities, making them candidates for drug development.
  • Research Tool: Compounds like 3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline are often used in research as molecular probes due to their unique reactivity.

Chemical Character

One of the striking features of this compound is the presence of the bromine substituent, which not only affects the compound's reactivity but also enhances its electronic properties. The methoxy group attached to the phenyl ring contributes to the compound's ability to interact with various biological systems.

Structure and Reactivity

The compound exhibits resonance stability due to the conjugated system formed by the aniline and methyleneamino groups. This aspect allows it to participate in various electrophilic aromatic substitution reactions and enhances its functionality as a building block in organic synthesis.

Research and Development

Scientists are continually exploring the properties of compounds like 3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline. Its unique attributes make it a valuable subject for studies in:

  • Material Science
  • Medicinal Chemistry
  • Green Chemistry

In summary, 3-bromo-N-[(4-methoxyphenyl)methyleneamino]aniline is more than just a chemical formula; it represents a pathway to innovation in multiple scientific realms.