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

Identification

Molecular formula

C₁₅H₁₇NOS

CAS number

171068-86-9

IUPAC name

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

State

At room temperature, 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanone is typically in a solid state, often appearing as a powder or crystalline form, which is characteristic of many similar organic compounds.

Melting point (Celsius)

56.00

Melting point (Kelvin)

329.15

Boiling point (Celsius)

395.00

Boiling point (Kelvin)

668.15

General information

Molecular weight

245.37g/mol

Molar mass

245.3440g/mol

Density

1.1563g/cm³

Appearence

This compound typically appears as a yellowish powder or crystals, depending on its formulation and purity. It should be stored in a cool and dry place to maintain its stability and appearance.

Comment on solubility

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

The solubility of 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanone can be influenced by various factors, including its molecular structure and the polarity of solvents. Generally, this compound exhibits a moderate level of solubility in organic solvents.

Factors Affecting Solubility:

Polarity: Due to the presence of the piperidyl group, which is relatively polar, it contributes to the compound's solubility characteristics.
Solvent Choice: The compound is likely to dissolve well in solvents such as dimethyl sulfoxide (DMSO) and ethanol, while having limited solubility in highly polar solvents like water.
Temperature: Increased temperature can often enhance the solubility of organic compounds, making it essential to consider thermal conditions during experiments.

As with many organic compounds, a rule of thumb is that "like dissolves like." Therefore, non-polar solvents may not be ideal for dissolving this compound efficiently.

Understanding the solubility of 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanone is crucial for its potential applications in both laboratory settings and drug formulation processes.

Interesting facts

Exploring 1-(Benzothiophen-3-yl)-2-(1-piperidyl)ethanone

1-(Benzothiophen-3-yl)-2-(1-piperidyl)ethanone is a fascinating compound with several intriguing characteristics and potential applications. As a derivative of benzothiophene, it incorporates a benzothiophene moiety, which is well-known for its diverse biological activities. Here are some interesting facts about this compound:

Biological Significance: Compounds containing benzothiophene structures have been reported to exhibit a variety of pharmacological effects, including anti-inflammatory, antioxidant, and anticancer properties.
Neurochemical Potential: The presence of the piperidine ring opens avenues for research into neurochemical interactions, suggesting possible benefits in the field of neuropharmacology.
Synthetic Versatility: The synthesis of such aromatic compounds can often be approached with various synthetic methodologies, showcasing the flexibility in organic chemistry.
Research Interest: Given the compound's structural features, it's a subject of interest in drug development, particularly for targeting specific enzymes or receptors in biological systems.

In conclusion, 1-(benzothiophen-3-yl)-2-(1-piperidyl)ethanone stands at the crossroads of organic chemistry and pharmacological research. As scholars delve into its properties and potential applications, the compound serves as a reminder of the complex relationships between chemical structure and biological activity, inviting further exploration and discovery.