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3-(piperidine-1-carbonyl)chromen-2-one

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Identification
Molecular formula
C15H15NO3
CAS number
60451-86-9
IUPAC name
3-(piperidine-1-carbonyl)chromen-2-one
State
State

At room temperature, this compound is in a solid state. It is usually handled as a fine powder, which is stable under normal conditions of use and storage.

Melting point (Celsius)
138.00
Melting point (Kelvin)
411.15
Boiling point (Celsius)
515.15
Boiling point (Kelvin)
788.30
General information
Molecular weight
271.31g/mol
Molar mass
271.3120g/mol
Density
1.3000g/cm3
Appearence

This compound appears as a crystalline solid with a yellowish or off-white color. It is typically found in powder form and may exhibit a slight sheen depending on the presence of crystalline structures. The precise appearance can vary depending on its purity and the specific conditions under which it was synthesized.

Comment on solubility

Solubility of 3-(piperidine-1-carbonyl)chromen-2-one

The solubility of 3-(piperidine-1-carbonyl)chromen-2-one can be quite variable depending on the solvent used and environmental conditions. Here are some key points to consider:

  • Polar Solvents: Generally, compounds with polar functional groups tend to exhibit better solubility in polar solvents like water and methanol. However, the presence of the piperidine ring may influence its overall polarity.
  • Non-Polar Solvents: On the other hand, 3-(piperidine-1-carbonyl)chromen-2-one might show higher solubility in non-polar solvents such as dichloromethane or chloroform due to the hydrophobic nature of its chromen-2-one structure.
  • Temperature Influence: The solubility may increase with temperature, as increased kinetic energy allows for greater interaction between solute and solvent molecules.
  • Saturation Points: It's essential to consider the saturation limits of this compound in various solvents, as exceeding these limits can lead to precipitation of the solute.

In summary, the solubility of 3-(piperidine-1-carbonyl)chromen-2-one is influenced by several factors including the choice of solvent, temperature, and the intrinsic properties of the molecule itself. Understanding these aspects can significantly aid in its practical applications.

Interesting facts

Exploring 3-(piperidine-1-carbonyl)chromen-2-one

3-(piperidine-1-carbonyl)chromen-2-one is a fascinating compound that belongs to the family of chromones, which are known for their diverse range of biological activities. Here are some intriguing facts about this compound:

  • Biological Relevance: Compounds like 3-(piperidine-1-carbonyl)chromen-2-one have been studied for their potential therapeutic properties, including anti-inflammatory and anticancer effects. Research shows that chromones can interact with various biological pathways, making them significant in medicinal chemistry.
  • Synthetic Versatility: The incorporation of the piperidine ring enhances the compound's structural diversity, opening avenues for modifying its properties. This versatility can lead to the creation of derivatives with tailored biological activities.
  • Fluorescence Properties: Many chromone derivatives possess unique fluorescence characteristics. This property is of great interest in the field of bioimaging and sensor technology, where these compounds could serve as effective probes.

As this compound illustrates, the field of synthetic organic chemistry provides ample opportunities for discoveries that bridge the gap between structural modification and functional applications. The exploration of such compounds not only deepens our understanding of chemical interactions but also expands the possibilities for innovative drug design.

Future Perspectives

Research into 3-(piperidine-1-carbonyl)chromen-2-one and its analogs could lead to:

  1. Development of novel pharmacological agents.
  2. Insights into structure-activity relationships for improved therapeutic efficacy.
  3. Enhanced understanding of natural product synthetics using chromone frameworks.

As the scientific community continues to investigate these compounds, we are likely to uncover even more remarkable functionalities that could benefit various fields, from medicine to materials science.

Synonyms
18144-51-9
3-(Piperidinocarbonyl)coumarin
COUMARIN, 3-(PIPERIDINOCARBONYL)-
BRN 0262898
DTXSID40171147
4-20-00-01321 (Beilstein Handbook Reference)
DTXCID5093638
3-(piperidine-1-carbonyl)-2H-chromen-2-one
3-(piperidine-1-carbonyl)chromen-2-one
3-(Piperidinocarbonyl)-2H-1-benzopyran-2-one
2H-1-Benzopyran-2-one, 3-(1-piperidinylcarbonyl)-
Maybridge3_000248
3-(piperidin-1-ylcarbonyl)-2H-chromen-2-one
Oprea1_179320
Oprea1_457811
HMS1431L06
3-(piperidylcarbonyl)chromen-2-one
STK760522
AKOS000533281
IDI1_011635
ST4047117
SR-01000410419
3-(1-PIPERIDINYLCARBONYL)-2H-CHROMEN-2-ONE
SR-01000410419-1
Z31424466