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

Identification

Molecular formula

C₁₅H₁₉NOS

CAS number

15168-05-5

IUPAC name

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

State

At room temperature, 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanol is in a solid state. It appears as a crystalline powder, characteristic of many organic compounds with similar structural features.

Melting point (Celsius)

97.40

Melting point (Kelvin)

370.50

Boiling point (Celsius)

442.30

Boiling point (Kelvin)

715.50

General information

Molecular weight

259.38g/mol

Molar mass

259.3610g/mol

Density

1.1923g/cm³

Appearence

The compound 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanol typically presents as a white to off-white crystalline powder. It is known for its crystalline nature and may exhibit a mild odor.

Comment on solubility

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

The solubility of the compound 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanol can be influenced by various factors such as temperature, pH, and the presence of solvents. Understanding its solubility characteristics is paramount for applications in pharmaceuticals and material sciences. Here are some important points to consider:

Polarity: The presence of the hydroxyl group (-OH) suggests that the compound may have a degree of polarity, which could enhance its solubility in polar solvents like water.
Hydrophobic Regions: The benzothiophene moiety can contribute to hydrophobic interactions, potentially lowering the solubility in aqueous environments.
Solvent Systems: It is likely to exhibit varying solubility in organic solvents. Common solvents such as ethanol and methanol might improve solubility due to similar polar characteristics.

It is critical to conduct empirical tests to ascertain the exact solubility parameters, as predicted outcomes can diverge from experimental data. For researchers and formulators, the insight into solubility can vastly affect the effectiveness and delivery of the compound in various applications.

Interesting facts

Interesting Facts about 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanol

The compound 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanol is a fascinating entity in the realm of organic chemistry, notable for its structural features and potential applications. This compound is derived from both benzothiophene, a fused bicyclic structure, and piperidine, which is a six-membered nitrogen-containing ring. Here are some engaging points about this compound:

Structural Significance: The presence of the benzothiophene moiety contributes to the compound's aromatic characteristics, affecting its reactivity and interactions with biological systems.
Biological Activity: Some studies suggest that compounds featuring piperidine structures may exhibit various pharmacological effects, making this compound a candidate for further research in drug development.
Versatile Synthesis: The synthesis of this compound may involve innovative reactions, broadening the understanding of synthetic methods in organic chemistry.
Research Potential: Given its interesting molecular architecture, this compound could serve as a valuable framework in medicinal chemistry, possibly leading to new therapeutic agents.

As scientists continue to explore the diverse functionalities of such compounds, understanding their properties can provide insights into their potential uses in various fields. This balances basic research with the exciting prospect of application in pharmaceuticals, materials science, and even agrochemicals.

In summary, 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanol embodies a unique intersection of structure and potential utility, paving the way for future discoveries.