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N,N-bis(2-bromoethyl)aniline

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Identification
Molecular formula
C10H13Br2N
CAS number
2188-82-1
IUPAC name
N,N-bis(2-bromoethyl)aniline
State
State
It is a liquid at room temperature, typically presented in its pure form as a colorless to yellow liquid, though impurities can give it a slight hue.
Melting point (Celsius)
11.00
Melting point (Kelvin)
284.00
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.00
General information
Molecular weight
319.00g/mol
Molar mass
318.9980g/mol
Density
1.6705g/cm3
Appearence

N,N-bis(2-bromoethyl)aniline appears as a pale yellow to yellow liquid. It might have a slight aromatic odor characteristic of aniline derivatives.

Comment on solubility

Solubility of N,N-bis(2-bromoethyl)aniline

N,N-bis(2-bromoethyl)aniline is a compound that exhibits interesting solubility characteristics, which can be influenced by several factors:

  • Polarity: As a molecule with both bromine and an amine functional group, it presents a mix of polar and non-polar characteristics, affecting its solubility in various solvents.
  • Solvent Interaction: Typically, this compound is likely to be soluble in organic solvents such as ethanol, chloroform, and dimethyl sulfoxide (DMSO), while being less soluble in polar protic solvents like water.
  • Hydrophobic Effects: The hydrocarbon chain contributes to hydrophobic interactions, which can limit its solubility in aqueous environments.

In summary, the solubility of N,N-bis(2-bromoethyl)aniline is a complex interplay between its chemical structure and the nature of the solvent. To evaluate its solubility practically, one must consider the specific conditions, such as temperature and solvent composition, which can significantly influence its behavior. As often stated, "Like dissolves like," which emphasizes the importance of matching the polarity of the solute and solvent for optimal solubility.

Interesting facts

Exploring N,N-bis(2-bromoethyl)aniline

N,N-bis(2-bromoethyl)aniline is an intriguing compound that offers a wealth of opportunities for scientific exploration. This compound, a derivative of aniline, is characterized by the presence of two bromoethyl groups attached to the nitrogen of the aniline moiety. Here are some remarkable aspects of this compound:

  • Structural Diversity: The unique structure of N,N-bis(2-bromoethyl)aniline allows it to participate in diverse chemical reactions, making it a versatile building block in organic synthesis.
  • Potential Applications: Its reactivity makes it a potential candidate in the development of pharmaceuticals and agrochemicals, particularly in areas where targeting specific biological pathways is essential.
  • Research Implications: Exploring this compound can yield insights into mechanisms of action and interactions with other chemical species, which is crucial for advances in medicinal chemistry.
  • Environmental Considerations: Given the presence of bromine, understanding the environmental persistence and degradation pathways of N,N-bis(2-bromoethyl)aniline is vital for assessing its ecological impact.

As stated by chemist Robert H. Grubbs, *“Chemistry is the art of transformation.”* This compound embodies the transformational potential of organic chemistry, making it a fascinating subject for both students and researchers alike. Studying N,N-bis(2-bromoethyl)aniline not only enhances knowledge of organic reactions but also underscores the importance of chemical safety and responsibility in scientific exploration.

Synonyms
N,N-Bis(2-bromoethyl)aniline
Benzenamine, N,N-bis(2-bromoethyl)-
2045-19-4
ANILINE, N,N-BIS(2-BROMOETHYL)-
NSC-260404
NSC 260404
BRN 0779106
NSC260404
VPA4GEU4QG
WLN: E2NR&2E
CHEMBL19482
Aniline,N-bis(2-bromoethyl)-
SCHEMBL11056830
n,n-bis[2-bromo-ethyl] aniline
DTXSID50174402
LTZFEVFXIMXNRW-UHFFFAOYSA-N
N,N-Bis(2-bromoethyl)benzenamine
Benzenamine,N-bis(2-bromoethyl)-