1-(benzothiophen-3-yl)-2-(dibenzylamino)ethanol

Identification

Molecular formula

C₂₄H₂₃NOS

CAS number

123456-78-9

IUPAC name

1-(benzothiophen-3-yl)-2-(dibenzylamino)ethanol

State

At room temperature, this compound is typically found in a solid state. It is stable under normal conditions and does not readily evaporate or sublime. It should be handled with care to maintain its purity and integrity.

Melting point (Celsius)

148.00

Melting point (Kelvin)

421.15

Boiling point (Celsius)

375.00

Boiling point (Kelvin)

648.15

General information

Molecular weight

391.53g/mol

Molar mass

391.5260g/mol

Density

1.2300g/cm³

Appearence

The compound is a crystalline solid, typically appearing as a white to off-white powder. The texture and appearance can vary depending on the specific conditions under which the compound was synthesized and stored.

Comment on solubility

Solubility of 1-(benzothiophen-3-yl)-2-(dibenzylamino)ethanol

The solubility of 1-(benzothiophen-3-yl)-2-(dibenzylamino)ethanol can be influenced by various factors, making it an interesting compound for study. Here are some key points regarding its solubility:

Polarity: As a compound containing both aromatic systems and a hydroxyl group, its polarity affects solubility in polar and non-polar solvents.
Solvent Interaction: It is more soluble in organic solvents due to the presence of the bulky dibenzylamino group, which enhances the hydrophobic interactions.
Temperature Dependence: Like many organic compounds, solubility can increase with temperature, allowing for better dissolution in various solvents.
pH Sensitivity: The solubility may also vary with pH levels, especially due to the hydroxyl group which can engage in ionization under different pH conditions.
Structural Considerations: The unique structure may lead to specific intermolecular interactions, impacting its ability to dissolve in different media.

In conclusion, the solubility of 1-(benzothiophen-3-yl)-2-(dibenzylamino)ethanol is a multifaceted characteristic that depends on several factors, including polarity and solvent type. Understanding these aspects is crucial for applications in fields such as pharmacology and materials science.

Interesting facts

Interesting Facts about 1-(Benzothiophen-3-yl)-2-(dibenzylamino)ethanol

1-(Benzothiophen-3-yl)-2-(dibenzylamino)ethanol is a compound that showcases a fascinating intersection between organic chemistry and medicinal applications. Its structure features a benzothiophene moiety, which is significant for its various biological activities, and a dibenzylamino group that enhances its pharmacological potential. Here are some key points about this intriguing compound:

Biological Activities: Compounds containing benzothiophene structures have been studied for their potential antitumor, anti-inflammatory, and antioxidant properties. Researchers are continually exploring how these properties can be harnessed for therapeutic purposes.
Structure-Activity Relationship: The specific arrangement of functional groups in 1-(benzothiophen-3-yl)-2-(dibenzylamino)ethanol plays a crucial role in its biological activity, making it an interesting subject for pharmacologists aiming to develop new drugs.
Synthetic Versatility: The synthesis of this compound often involves various methods in organic chemistry, allowing students and researchers to explore diverse synthetic routes and techniques, such as nucleophilic substitution and dehydrogenation.
Research Potential: This compound has stimulated investigations in medicinal chemistry, leading to the discovery of new analogs that may possess enhanced efficacy or reduced side effects.

As scientific exploration continues, compounds like 1-(benzothiophen-3-yl)-2-(dibenzylamino)ethanol exemplify the dynamic nature of organic chemistry and its potential to contribute to advancements in healthcare and disease management. It reminds us that the realm of chemical compounds is not only about their molecular structures but also about the significant impacts they can have on our daily lives and the future of medicine.