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2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine

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Identification
Molecular formula
C11H15BrClN
CAS number
28578-16-7
IUPAC name
2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine
State
State

At room temperature, 2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine is in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
262.60g/mol
Molar mass
262.5990g/mol
Density
1.3350g/cm3
Appearence

2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine typically appears as a colorless to pale yellow liquid.

Comment on solubility

Solubility of 2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine

The solubility of 2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine can be influenced by various factors, including temperature, solvent choice, and molecular interactions. Here are some key points regarding its solubility:

  • Organic Solvents: This compound is likely to have significant solubility in organic solvents due to its hydrophobic aromatic groups and ethyl substitution.
  • Water Solubility: Given its structural characteristics, including bromine and chlorine substituents, the water solubility may be limited.
  • Influence of Temperature: The solubility may increase with rising temperature, as higher temperatures typically enhance molecular mobility.
  • Interactions: The presence of halogens (bromine and chlorine) may engage in dipole-dipole interactions, potentially impacting solubility in polar solvents.

In conclusion, the solubility profile of 2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine is dictated primarily by its functional groups and the nature of the solvent, which can result in varying degrees of solubility based on environmental conditions.

Interesting facts

Interesting Facts about 2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine

2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine, commonly referred to in the field of chemistry for its unique structure and properties, presents a fascinating subject of study. This compound falls under the category of aminomethyl derivatives, which are of great interest due to their applications in various fields, including pharmacology and materials science.

Chemical Properties

One noteworthy aspect of this compound is its bromine atom substitution, which greatly influences its reactivity. The presence of the bromine atom can enhance electrophilicity, allowing it to engage in a variety of reactions such as:

  • Halogenation
  • Nucleophilic substitutions
  • Formation of organometallic complexes

Biological Significance

From a biological perspective, compounds like this one are often studied for their potential therapeutic applications. Here are some critical points regarding their biological relevance:

  • Many aminomethyl derivatives possess significant antidepressant and anxiolytic properties.
  • The specific presence of the chlorophenyl group may enhance binding affinity to certain receptors.
  • Compounds similar to this one are often evaluated for their role in neurotransmitter regulation.

Synthetic Pathways

The synthesis of 2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine can involve various reaction pathways, including:

  • The introduction of the bromine atom through electrophilic aromatic substitution.
  • Utilization of amine chemistry to create the desired functional groups.

Such synthetic routes not only highlight the compound's synthetic versatility but also provide insight into the broader synthesis of related heterocyclic compounds.

In summary, the compound 2-bromo-N-[(4-chlorophenyl)methyl]-N-ethyl-ethanamine illustrates the beautiful complexity of organic chemistry, showcasing how subtle changes in structure can lead to vastly different chemical behaviors and potential applications.

Synonyms
N-(2-Bromoethyl)-p-chloro-N-ethylbenzylamine
BENZYLAMINE, N-(2-BROMOETHYL)-p-CHLORO-N-ETHYL-
19928-02-0
DTXSID40173707
DTXCID0096198
RefChem:328805
AKOS019246297