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2-(9-anthryl)-N,N-dimethylethanamine

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Identification
Molecular formula
C18H19N
CAS number
92480-07-4
IUPAC name
2-(9-anthryl)-N,N-dimethyl-ethanamine
State
State

At room temperature, 2-(9-Anthryl)-N,N-dimethylethanamine is in a solid state. The compound is typically handled in its crystalline form for practical applications, including research and synthesis purposes.

Melting point (Celsius)
57.00
Melting point (Kelvin)
330.15
Boiling point (Celsius)
353.00
Boiling point (Kelvin)
626.15
General information
Molecular weight
251.35g/mol
Molar mass
251.3490g/mol
Density
1.0650g/cm3
Appearence

2-(9-Anthryl)-N,N-dimethylethanamine typically appears as a crystalline solid. The compound can range in color from pale yellow to tan, depending on its purity and form. It might exhibit fluorescence under UV light due to the anthryl group.

Comment on solubility

Solubility of 2-(9-anthryl)-N,N-dimethyl-ethanamine

2-(9-anthryl)-N,N-dimethyl-ethanamine, often characterized by its aromatic structure, presents interesting solubility properties that are heavily influenced by its molecular characteristics. Generally, it is considered poorly soluble in water due to its large hydrophobic anthracene ring, which tends to limit interactions with polar solvents.

Key factors influencing its solubility include:

  • Aromatic structure: The aromatic segment of the compound enhances its lipophilicity, making it more soluble in organic solvents.
  • Alkyl groups: The N,N-dimethyl groups introduce some degree of polarity, but not enough to significantly enhance solubility in aqueous environments.
  • Hydrogen bonding: While there may be potential for hydrogen bonding with protic solvents, the steric hindrance presented by the bulky groups reduces these interactions.

In general, expect the compound to dissolve more readily in organic solvents such as:

  • Dimethyl sulfoxide (DMSO)
  • Ethanol
  • Toluene

As a concluding note, the solubility of 2-(9-anthryl)-N,N-dimethyl-ethanamine can be summarized as follows: it is lipophilic and prefers non-polar or slightly polar solvents over water, highlighting the balance between hydrophobic and polar interactions in organic molecules.

Interesting facts

Exploring 2-(9-anthryl)-N,N-dimethyl-ethanamine

2-(9-anthryl)-N,N-dimethyl-ethanamine, often known for its fascinating structural chemistry, brings together unique elements that make it a compound of interest in various fields of study. Here are several intriguing aspects:

  • Fluorescent Properties: Due to the presence of the anthracene moiety, this compound exhibits notable fluorescence, making it useful in organic light-emitting diodes (OLEDs) and other optoelectronic applications.
  • Biological Activity: Compounds with similar amine structures have been explored for their potential as neurotransmitter modulators, thus sparking interest in their roles in neurochemical research.
  • Synthetic Utility: The synthesis of 2-(9-anthryl)-N,N-dimethyl-ethanamine incorporates straightforward methods often used in organic synthesis, allowing chemists to utilize this compound as a building block in the development of more complex molecules.
  • Structure-Activity Relationship: By modifying the alkyl groups or the anthracene core, researchers can extensively study the relationship between structure and function, leading to discoveries in medicinal chemistry.
  • Polymer Science: With its potential for incorporation into polymer matrices, this compound may enhance the performance of materials, making it significant in the development of advanced materials with tailored properties.

As with many complex organic compounds, 2-(9-anthryl)-N,N-dimethyl-ethanamine serves as a reminder of the intricate connections between structure, properties, and applications in the realm of chemistry. "The study of chemical compounds is the study of life's toolbox," we often say, and this compound illustrates just how versatile that toolbox can be.