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2-(Dimethylamino)-1-(1-naphthyl)ethanol

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Identification
Molecular formula
C14H17NO
CAS number
13171-18-1
IUPAC name
2-(dimethylamino)-1-(1-naphthyl)ethanol
State
State

This compound is generally found in a solid state at room temperature, although it can also exist in a very viscous liquid form depending on its environment and handling.

Melting point (Celsius)
79.00
Melting point (Kelvin)
352.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
201.28g/mol
Molar mass
201.2820g/mol
Density
1.1343g/cm3
Appearence

2-(Dimethylamino)-1-(1-naphthyl)ethanol typically appears as a colorless to pale yellow solid or viscous liquid. The compound may form crystals, depending on purity and storage conditions.

Comment on solubility

Solubility of 2-(dimethylamino)-1-(1-naphthyl)ethanol

The solubility of 2-(dimethylamino)-1-(1-naphthyl)ethanol is an intriguing aspect that can influence its applications in various fields. This compound exhibits variable solubility characteristics, primarily due to its molecular structure.

Key Factors Affecting Solubility

  • Polarity: The presence of the dimethylamino group renders the compound relatively polar, which can enhance its solubility in polar solvents like water and alcohols.
  • Hydrophobic nature: The naphthyl group, being largely non-polar, contributes to hydrophobic interactions, often reducing the overall solubility in aqueous environments.
  • Solvent interactions: The solubility is also influenced by the choice of solvent, as 2-(dimethylamino)-1-(1-naphthyl)ethanol may dissolve more readily in organic solvents like dichloromethane or ethanol compared to water.

As a rule of thumb, the overall solubility can often be described by the phrase, “like dissolves like”, indicating that the compound is likely to be more soluble in solvents with similar polarities.

In conclusion, while 2-(dimethylamino)-1-(1-naphthyl)ethanol can show promising solubility in appropriate solvents, it is essential to consider both the polar and non-polar characteristics when predicting its behavior in various chemical environments.

Interesting facts

2-(Dimethylamino)-1-(1-naphthyl)ethanol: A Closer Look

This fascinating compound, known as 2-(dimethylamino)-1-(1-naphthyl)ethanol, has garnered interest in various fields due to its unique structural features and biological activities. Here are some interesting facts that highlight its significance:

  • Structure and Function: The compound possesses a distinctive structure that includes a dimethylamino group, which contributes to its pharmacological properties. The presence of the naphthyl group enhances its ability to interact with biological systems.
  • Pharmacological Potential: Researchers have investigated this compound for its potential applications in drug development, particularly in the treatment of neurological disorders. Its molecular structure suggests it may exhibit effects similar to those of well-known psychoactive substances.
  • Research Applications: In laboratory settings, it serves as a useful intermediate in organic synthesis and can be explored in the development of novel materials and chemical processes.
  • Biological Interactions: The compound can act on various receptors in the central nervous system, making it a subject of study for its possible roles in modulating neurotransmitter activity. This opens avenues for exploring its impact on mood and cognitive functions.
  • Unique Properties: Due to the combination of an aromatic naphthyl ring and a versatile amino-alcohol functional group, it exhibits a range of reactivity that can be harnessed in chemical reactions, paving the way for new synthetic methodologies.

As a chemical scholar or enthusiast, understanding compounds like 2-(dimethylamino)-1-(1-naphthyl)ethanol not only enhances our grasp of chemistry but also illuminates the intricate connections between molecular structure and biological function. With ongoing research, it is exciting to speculate on the potential breakthroughs that may arise from this compound in the future.

Synonyms
AKOS011033493