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N-(2-Bromoethyl)aniline

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Identification
Molecular formula
C8H10BrN
CAS number
694-80-4
IUPAC name
N-(2-bromoethyl)aniline
State
State
At room temperature, N-(2-bromoethyl)aniline is typically in a liquid state. It is commonly handled as a liquid for its use in chemical synthesis and potential applications in pharmaceuticals.
Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
261.00
Boiling point (Kelvin)
534.15
General information
Molecular weight
200.08g/mol
Molar mass
200.0640g/mol
Density
1.4510g/cm3
Appearence

N-(2-Bromoethyl)aniline appears as a colorless to pale yellow liquid. It is typically slightly viscous and oily, and it may darken upon exposure to air or light due to slow oxidation.

Comment on solubility

Solubility of N-(2-bromoethyl)aniline

N-(2-bromoethyl)aniline, with its unique structure, exhibits interesting solubility characteristics in various solvents. Understanding its solubility can provide insights into its practical applications and behavior in chemical processes. Here are some key points regarding its solubility:

  • Polar Solvents: N-(2-bromoethyl)aniline tends to be more soluble in polar solvents such as water and alcohols due to its amino group, which can engage in hydrogen bonding.
  • Non-Polar Solvents: In contrast, its solubility in non-polar solvents like hexane or benzene may be limited due to the polar nature of the amine and bromoethyl functional groups.
  • Temperature Influence: The solubility can also vary with temperature; generally, an increase in temperature enhances solubility for many compounds.
  • Concentration Effects: At higher concentrations, the solubility may exhibit saturation behavior, which can lead to precipitation if the solvent cannot accommodate the excess compound.

As a general observation, the interplay of polarity and structural features greatly influences the solubility of N-(2-bromoethyl)aniline.
Understanding these solubility properties is crucial for any applications involving this compound, such as in synthesis or formulation processes.

Interesting facts

Interesting Facts About N-(2-bromoethyl)aniline

N-(2-bromoethyl)aniline is an intriguing compound in the realm of organic chemistry, especially due to its applications in various fields such as pharmaceuticals and materials science. Here are some fascinating aspects of this compound:

  • Structural Features: This compound features a unique combination of an aniline ring and a bromoethyl side chain. The presence of the bromine atom not only imparts certain reactivity but also influences the compound's physical and chemical properties.
  • Reactivity: The bromoethyl group makes N-(2-bromoethyl)aniline a potential candidate for nucleophilic substitution reactions. This reactivity opens pathways for the formation of more complex molecules through further chemical transformations.
  • Biological Activity: Compounds similar to N-(2-bromoethyl)aniline exhibit interesting biological activities. They can serve as intermediates in the synthesis of anti-cancer agents and other therapeutic drugs, highlighting their significance in medicinal chemistry.
  • Synthesis Routes: There are various methods to synthesize N-(2-bromoethyl)aniline, including reactions involving haloalkanes and amines. Understanding these synthesis routes is fundamental for chemists looking to produce this compound efficiently.
  • Industrial Applications: Beyond its pharmaceutical implications, this compound can also be utilized in the production of specialty polymers and dyes, demonstrating its versatility in industrial settings.

As a compound, N-(2-bromoethyl)aniline exemplifies how a simple modification of a basic aniline structure can lead to compounds with significant functionality and applications. The study of such compounds can pave the way for novel discoveries in both academic and industrial chemistry.

Synonyms
N-(2-Bromoethyl)aniline
XG5YZQ6RPR
Benzenamine, N-(2-bromoethyl)-
EINECS 211-827-3
AI3-52956
DTXSID90220179
N-(2-BROMOETHYL)BENZENAMINE
DTXCID40142670
211-827-3
699-11-6
UNII-XG5YZQ6RPR
SCHEMBL2005814
AQRDPQOVPUDAQO-UHFFFAOYSA-N
AKOS002391980
CS-0367699
NS00036979